Stryker Corporation
FDA 510(k) & PMA Approved Devices — 43 products
Total Devices43
Categories24
Latest FDA decision2023-08-18
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K151932 | Stryker CrossFlow Day-Use Inflow Cassette Tubing and Patient-Use Tubing | HRX | 2016-03-31 | View |
| 510(k) | K153679 | Stryker Neptune E-SEP Smoke Evacuation Pencil | GEI | 2016-01-22 | View |
| 510(k) | K151726 | AVS AL and AVS ALign PEEK Spacers, AVS PL and AVS UniLIF PEEK Spacers, AVS TL PEEK Spacer, AVS Navigator PEEK Spacer, AVS ARIA PEEK Spacer | MAX | 2016-01-20 | View |
No matching devices.
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