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The Laminar Shaping Plate Instrument Set from Peak Surgicals is a 20-piece cervical spine instrumentation set designed for the complete intraoperative workflow of laminoplasty plate shaping, sizing, and application during open-door or French-door cervical laminoplasty surgery. The set covers all steps from laminar plate size selection using five Mold Trials (4–12mm), cortical drilling with five 1.5mm Hand Drill Bits matched to the five plate thicknesses, plate bending and cutting with two dedicated Bending Cutting Forceps, plate positioning and holding with two Plate Holding Forceps and a Plate Holding Clamp, laminar cortex entry with an AWL, and final screw insertion with two Screwdrivers, all supplied in a Plate Box and an aluminium box. It is used by spine surgeons and neurosurgeons in hospital operating theatres performing cervical laminoplasty for cervical spondylotic myelopathy, ossification of the posterior longitudinal ligament (OPLL), and multilevel cervical stenosis requiring expansion of the cervical spinal canal while preserving the posterior spinal elements.
Cervical laminoplasty is a posterior cervical decompression technique in which the cervical spinal canal is enlarged by hinging or dividing the posterior arch of the cervical vertebrae — the laminae — without removing them, thereby preserving the posterior tension band and reducing the risk of postoperative instability and axial pain compared to laminectomy. In open-door laminoplasty, the laminae are cut on one side (the open side) and hinged on the opposite side (the hinge side), and a spacer plate — the laminoplasty plate — is inserted into the open-door gap to hold the opened lamina in its expanded position while bony fusion occurs across the hinge and at the plate attachment. The laminoplasty plate must be bent intraoperatively to match the individual patient's laminar angle and gap size, which varies with the vertebral level and the degree of spinal canal expansion required. The Mold Trials in this set allow the surgeon to select the correct plate height for each level before the plate is prepared, and the Bending Cutting Forceps allow the plate to be contoured and trimmed to the required shape without damaging the plate material. The Hand Drill Bits (1.5mm) provide the small cortical pilot holes required for the plate-securing screws in the laminar cortex, where the available bone thickness is limited and precise small-diameter drilling is essential to avoid cortical perforation.
The five Mold Trials (PS-MT-0007 to PS-MT-0011, 4mm/6mm/8mm/10mm/12mm) allow the surgeon to confirm the correct laminoplasty plate height for each spinal level before the definitive plate is prepared and applied. After the open-door cut is completed and the lamina is hinged open, the Mold Trial for each level is inserted into the open-door gap and assessed for fit — the trial must seat stably in the gap without rocking or migrating, provide the targeted degree of spinal canal expansion confirmed on intraoperative fluoroscopy, and not extend beyond the cortical surface at the plate attachment points. The height range of 4–12mm covers the full spectrum of open-door gaps used in clinical cervical laminoplasty, from single-level cases in younger patients with smaller canal dimensions to multilevel OPLL cases where larger expansion distances are required. Once the appropriate trial size is confirmed for each level, the matching definitive plate is selected from the Plate Box and prepared using the Bending Cutting Forceps.
The five Hand Drill Bits (PS-HDB-0002 to PS-HDB-0006, 1.5mm diameter × 4mm, 6mm, 8mm, 10mm, 12mm depths) provide the pilot hole drilling matched to each of the five plate sizes. The 1.5mm drill diameter is specifically sized for the small-diameter cortical screws used in laminoplasty plate fixation, where the laminar cortex is typically only a few millimetres thick and requires a precise pilot hole to guide the screw without cortical splitting or laminar fracture. The five length options correspond to the five mold trial heights — a longer drill is needed when the plate spacer creates a deeper gap between the laminar edge and the adjacent bone where the plate is secured — ensuring the pilot hole depth is matched to the plate configuration at each level. Manual hand drill operation, rather than power drilling, allows the surgeon to feel the cortical resistance and stop precisely at the required depth without over-drilling in the limited laminar bone stock available in cervical laminoplasty.
The two Bending Cutting Forceps (PS-BCF-0012 and PS-BCF-0013) serve dual functions: bending the laminoplasty plate to match the required curvature of the laminar surface at each level, and cutting the plate to the required length if trimming is needed. Laminoplasty plates are supplied as straight segments and must be contoured intraoperatively to follow the curvature of the laminar surface and the angle of the open-door gap — the Bending Cutting Forceps allow controlled bending without creasing or weakening the plate material. The two Plate Holding Forceps (PS-PHF-0014 and PS-PHF-0015) grip the bent plate during positioning in the open-door gap, maintaining its orientation against the laminar surface while the AWL creates the initial screw entry point and the first screws are inserted. The Plate Holding Clamp (PS-PHC-0016) holds the plate clamped against the laminar bone surface without requiring the surgeon to maintain manual forcep pressure, freeing both hands for drilling and screw insertion. The AWL (PS-AWL-0017) creates the initial cortical entry point at the screw site before the Hand Drill Bit is advanced, providing a guided start for the small-diameter drill in the curved cortical surface. The two Screwdrivers (PS-S-0018 and PS-S-0019) provide the final screw insertion torque for the plate-securing screws.
The Laminar Shaping Plate Instrument Set is manufactured under CE Mark, ISO 13485, and FDA compliant quality standards. ISO 13485 certification confirms Peak Surgicals operates a documented quality management system covering design control, material traceability, and production consistency for spinal surgical instruments. CE Mark confirms conformity with European medical device regulations, and FDA compliance supports procurement for US-based hospitals, spine surgery centers, and neurosurgical departments requiring verified regulatory documentation for cervical laminoplasty instrumentation purchases.
| SKU | — (verify in Shopify admin) |
|---|---|
| Product Name | Laminar Shaping Plate Instrument Set |
| Price | $1,650.00 USD |
| Total Items | 20 items + Aluminium Box |
| Instrument Category | Spine Surgery — Cervical Laminoplasty Plate Shaping and Application |
| Procedure | Open-door cervical laminoplasty for cervical spondylotic myelopathy, OPLL, multilevel cervical stenosis |
| Plate Box | PS-PB-0001 (contains definitive laminoplasty plates) |
| Hand Drill Bits | 1.5mm × 4mm (PS-HDB-0002), 6mm (0003), 8mm (0004), 10mm (0005), 12mm (0006) — 5 total |
| Mold Trials | 4mm (PS-MT-0007), 6mm (0008), 8mm (0009), 10mm (0010), 12mm (0011) — 5 total |
| Bending Cutting Forceps | PS-BCF-0012, PS-BCF-0013 (×2) |
| Plate Holding Forceps | PS-PHF-0014, PS-PHF-0015 (×2) |
| Plate Holding Clamp | PS-PHC-0016 (×1) |
| AWL | PS-AWL-0017 (×1) |
| Screwdrivers | PS-S-0018, PS-S-0019 (×2) |
| Container | Aluminium Box (PS-AB-0020) |
| Certifications | CE Mark, ISO 13485, FDA |
| Warranty | 1 Year |
| MOQ | 1 Set |
| OEM / Custom Orders | Available |
| After-Sale Service | Return and Replacement |
What is cervical laminoplasty and when is it performed instead of laminectomy?
Cervical laminoplasty is a posterior cervical decompression procedure in which the cervical spinal canal is expanded by opening and propping the laminae — the posterior arches of the cervical vertebrae — rather than removing them. It is performed for multilevel cervical cord compression from cervical spondylotic myelopathy, OPLL, or developmental canal stenosis where decompression over three or more levels is required and the surgeon wishes to preserve the posterior spinal elements. Laminoplasty is preferred over laminectomy in this context because it maintains the posterior tension band of the spine (the laminae and attached ligaments and muscles), reducing the risk of postoperative kyphotic deformity and instability that can occur after multi-level laminectomy. Open-door laminoplasty hinges the laminae open on one side and holds the open gap with a spacer plate, while French-door laminoplasty splits the laminae centrally and opens them bilaterally; the Laminar Shaping Plate Instrument Set from Peak Surgicals is used primarily for open-door laminoplasty plate application.
What is the purpose of the Mold Trials and how are the five sizes selected intraoperatively?
The five Mold Trials (4mm, 6mm, 8mm, 10mm, 12mm) allow the surgeon to determine the correct laminoplasty plate height for each level before the definitive plate is prepared. After the open-door cut and hinge have been completed and the lamina is held open at the targeted expansion angle, the smallest appropriate trial is inserted into the open-door gap. The trial must seat stably at the laminar hinge without gapping or compression, provide the target degree of canal expansion confirmed fluoroscopically, and allow the plate attachment points on the laminar edge and the lateral mass to align correctly. Most single-level adult cases use a 6mm or 8mm plate height; larger expansion distances (10mm or 12mm) are used in severe OPLL or large-canal-diameter adults; 4mm may be used at C3 or for smaller patients. Confirming the mold trial before plate preparation prevents unnecessary plate contouring and reduces the risk of selecting a plate height that cannot be secured without cortical breach at the narrow laminar attachment points.
Why are 1.5mm hand drill bits used rather than standard power drill bits for laminoplasty plate screw holes?
The 1.5mm diameter is matched to the small cortical screws used in laminoplasty plate fixation, which are typically 1.5mm or 2.0mm diameter — the smallest orthopaedic screws used in any spinal surgery, reflecting the limited available bone volume in the cervical laminar cortex. Power drilling is generally avoided for these pilot holes for two reasons: first, the cervical laminar cortex is only 2–4mm thick and a power drill can easily advance through both cortices and into the spinal canal in milliseconds without the tactile feedback needed to stop at the correct depth; second, the small 1.5mm drill is prone to deflection and breakage under the torque of a power drill in the curved cortical surface. Manual hand drilling with the dedicated hand drill bits provides the controlled, low-speed cortical penetration needed to achieve a precise pilot hole at the correct depth without laminar fracture or inadvertent canal entry.
What is the role of the Plate Holding Clamp compared to the Plate Holding Forceps?
The two Plate Holding Forceps (PS-PHF-0014 and PS-PHF-0015) grip the bent laminoplasty plate from the ends during initial positioning in the open-door gap, allowing the surgeon to manoeuvre the plate into its correct orientation against the laminar surface while both forceps are under manual control. Once the plate is in the correct position, the Plate Holding Clamp (PS-PHC-0016) clamps the plate securely against the laminar bone surface at the mid-plate position, holding it stably without requiring the surgeon or assistant to maintain forcep pressure. This frees both of the surgeon's hands for the AWL cortical entry and Hand Drill Bit pilot hole creation and screw insertion steps, during which any movement of the plate would misalign the drill trajectory relative to the plate screw holes.
What certifications does this set carry?
The Laminar Shaping Plate Instrument Set is manufactured under CE Mark, ISO 13485, and FDA compliant quality standards. ISO 13485 certification confirms Peak Surgicals operates a documented quality management system covering design control, material traceability, and manufacturing consistency for spinal surgical instruments. CE Mark confirms conformity with European medical device regulations, and FDA compliance supports procurement for US hospitals, spine surgery centers, and neurosurgical departments requiring verified regulatory documentation for cervical laminoplasty instrumentation purchases.
Can individual instruments be ordered as replacements?
Individual instruments — Hand Drill Bits by length (PS-HDB-0002 to 0006), Mold Trials by size (PS-MT-0007 to 0011), Bending Cutting Forceps, Plate Holding Forceps, Plate Holding Clamp, AWL, and Screwdrivers — are available from Peak Surgicals as replacement items using their PS reference numbers. OEM manufacturing and custom set configurations are available for spine surgery centers and distributors. Contact Peak Surgicals directly for replacement instrument pricing, OEM specifications, or institutional procurement arrangements.
Order Processing: We strive to serve you promptly! Orders placed before the cut-off time of 5:00 PM (GMT -05:00) (Eastern Standard Time) will be processed the same business day. Orders placed after this time will be processed the next business day.
Handling Time: Our standard handling time is 1-2 business days (Monday through Friday). This includes order verification, quality checks, packaging, and dispatch. Please note that orders placed on weekends or holidays will be processed on the following business day.
Transit Time: Once dispatched, the estimated transit time is 4-5 business days (Monday through Friday). However, transit times may vary depending on your location and any unforeseen circumstances.
Shipping Fee: Enjoy free worldwide shipping on all orders over $250! At Peak Surgical Instruments, we cover all import charges for your convenience.
Customers will receive a tracking ID as soon as their order is dispatched via FedEx or DHL.
We proudly offer worldwide shipping, ensuring that our premium surgical instruments are accessible to healthcare professionals across the globe. No matter where you are, you can count on us to deliver quality tools right to your doorstep!
To provide you with confidence in your purchase, we offer a 1-year warranty as well as a 30-day money-back guarantee on all non-personalized orders.
We understand that delays can be frustrating. Transit times are estimates based on recent orders and may change. If your package is delayed, we will do everything possible to expedite delivery. In case of significant delays or missing packages, we will reship your order at no extra cost to you.
At Peak Surgicals, customer satisfaction and product quality are important to us. We offer a straightforward 30-day return policy, allowing eligible items to be returned within 30 days of delivery.
To qualify for a return, the item must be unused, in its original condition, and returned in the original packaging with tags, labels, and proof of purchase included.
Items must not show signs of use, alteration, damage, sterilization, or clinical handling after delivery.
To start a return, please contact us at info@peaksurgicals.com with your order number, product details, and reason for return.
Approved returns should be sent to:
Peak Surgicals
364 E Main Street
Middletown, DE 19709
Delaware, United States
No Restocking Fee: We do not charge restocking fees on approved returns.
Free Returns: If the item is incorrect, defective, or damaged during shipping, Peak Surgicals will cover the return shipping cost.
Customer Responsibility: If the customer ordered the wrong item or no longer needs the product, the customer is responsible for the return shipping cost.
Returned products must be received in new, unused condition with all labels, packaging, and documentation intact. Items that are used, damaged, altered, incomplete, or returned without approval may not be eligible for a refund.
Once your return is received and inspected, we will notify you whether the refund has been approved. Approved refunds will be processed to the original payment method within 10 business days.
Please note that your bank or credit card provider may require additional time to post the refund to your account.
Please inspect your order immediately after delivery. If your item is defective, damaged, or incorrect, contact us at info@peaksurgicals.com as soon as possible with your order number and clear photos of the product and packaging.
Certain items may not be eligible for return, including customized products, personalized instruments, special-order items, clearance items, sale items, and gift cards.
For exchanges, please return the original item after approval and place a new order for the replacement item. This helps ensure faster processing and accurate product selection.
Peak Surgicals supplies surgical, dental, orthopedic, gynecology, and veterinary instruments to healthcare professionals, clinics, hospitals, distributors, and procurement buyers worldwide.
For orders shipped to the European Union, customers may have the right to cancel or return an eligible order within 14 days of receipt, provided the item is unused, in its original condition, and returned with all original packaging and proof of purchase.
For return, refund, or exchange inquiries, please contact us:
Phone: +1 315 526 9968
Email: info@peaksurgicals.com