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PEAK SURGICAL
SKU:PS-O T-01506
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The Synovectomy Rongeurs are specialized orthopedic surgical instruments designed for controlled removal of synovial tissue during synovectomy procedures. Their rongeur-style working mechanism provides a dedicated instrument for grasping and excising thickened or diseased synovium within joint and tendon-sheath surgical fields.
The current Peak Surgicals product is manufactured from German stainless steel and is listed as reusable. The live storefront provides a Size selector, while satin, dull, and mirror finish options are stated in the current product specification.
A synovectomy involves surgical removal of synovial tissue from a joint or associated tendon sheath. A dedicated synovectomy rongeur provides the surgeon with a controlled instrument for progressively engaging and excising selected synovial tissue during the procedure.
This function should be distinguished from conventional bone rongeurs, which are primarily designed to bite or remove mineralized bone. The exact tissue targeted and extent of excision should be determined by the operating surgeon according to the procedure and pathology being treated.
Synovectomy rongeurs are used within orthopedic surgical instrument sets for procedures involving inflamed, thickened, or otherwise abnormal synovial tissue within a joint.
The exact joint, surgical approach, and working technique depend on the clinical procedure. The current Peak Surgicals page does not assign this particular model to a single joint or anatomical location.
The principal function of a synovectomy rongeur is to engage and remove selected synovial tissue in a controlled manner. This specialized function makes it useful where a dedicated tissue-excision instrument is required within a confined orthopedic operative field.
The current Peak Surgicals page does not provide exact jaw geometry, jaw width, curvature, or cutting-edge dimensions for this product. These specifications should therefore be confirmed before ordering when a particular working-end design is required.
The current product specification confirms German stainless steel construction. The metallic design provides the structural rigidity required for a reusable manually operated surgical rongeur.
The exact stainless-steel alloy grade is not stated on the current product page. Hospitals, orthopedic centers, distributors, and procurement teams requiring a specific steel designation or material certificate should confirm that information before ordering.
Peak Surgicals specifically identifies the Synovectomy Rongeurs as reusable. The instrument is intended for repeated professional use when appropriately cleaned, inspected, and reprocessed according to applicable manufacturer instructions and the healthcare facility's validated procedures.
Particular attention should be given to the working jaws, joint, and other areas where tissue debris may remain. Before reuse, the instrument should be inspected for jaw misalignment, cutting-edge damage, corrosion, restricted movement, deformation, or other visible deterioration.
The live Peak Surgicals storefront includes a Size selector for this product, indicating that selectable configurations are available.
However, the exact size values are not exposed in the currently accessible product information. Buyers requiring a specific overall length, jaw width, curvature, or working-end configuration should confirm the selected variant before ordering.
The current Peak Surgicals specification lists satin, dull, and mirror finish options. These allow hospitals, surgical centers, distributors, and procurement teams to select the required surface finish for their instrument inventory.
If a particular finish is required, it should be confirmed when placing the order.
Peak Surgicals lists this instrument for Operating Room and other professional surgical use. The product can be incorporated into orthopedic surgical sets requiring a dedicated synovectomy rongeur.
The current page does not provide a verified ratchet configuration, handle style, spring mechanism, working-end curvature, or procedure-specific size. These details should not be assumed from another manufacturer's synovectomy rongeur.
| Product Name | Synovectomy Rongeurs |
| Storefront Identifier | PS-O T-01506 |
| Model Number in Description | PS-9408 |
| Instrument Type | Synovectomy Rongeur |
| Primary Function | Controlled Synovial Tissue Removal |
| Specialty Context | Orthopedic Surgery |
| Material | German Stainless Steel |
| Feature | Reusable |
| Finish Options | Satin, Dull, Mirror |
| Listed Usage | Operating Room, Others |
| Size Options | Selectable – Exact Values Not Exposed on Current Page |
| Exact Jaw Dimensions | Not Specified on Current Product Page |
| Jaw Curvature | Not Specified on Current Product Page |
The Synovectomy Rongeurs are relevant for orthopedic departments, hospitals, joint surgery services, surgical centers, medical instrument distributors, and procurement teams sourcing reusable instruments for synovectomy procedures.
For accurate purchasing and inventory identification, buyers should confirm the correct product code because the current storefront displays PS-O T-01506 while the description lists PS-9408. Buyers requiring exact overall length, jaw width, jaw curvature, handle configuration, or stainless-steel alloy grade should also confirm those specifications before ordering.
They are specialized surgical instruments used for controlled removal of synovial tissue during synovectomy procedures.
No. A dedicated synovectomy rongeur is primarily intended for excision of synovial tissue, while conventional bone rongeurs are designed primarily for biting and removing bone.
The current Peak Surgicals specification identifies German stainless steel. The exact alloy grade is not stated.
Yes. The current Peak Surgicals listing specifically identifies the instrument as reusable.
The live storefront provides a Size selector, but the exact selectable dimensions are not exposed in the current product information.
The current storefront displays PS-O T-01506, while the existing description lists PS-9408. This discrepancy should be verified in Shopify before the product record is finalized.