Arthrex Arthroscopy Instruments, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
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Total Devices2
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K881792 | CANNULA MODEL AR-6551 | HRX | 1988-07-07 | View |
| 510(k) | K880295 | CANNULA MODEL AR-6001 | HRX | 1988-06-29 | View |
No matching devices.
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