Tenon Medical, Inc.
FDA 510(k) & PMA Approved Devices — 2 products
Total Devices2
Categories1
Latest FDA decision2023-08-24
SEC Filings: 1 filings on record. Latest: 8-K (2026-08-24). View on SEC EDGAR →
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K231944 | CATAMARAN SI Joint Fusion System | OUR | 2023-08-24 | View |
| 510(k) | K180818 | Catamaran Sacroiliac Joint Fixation System (CAT SIJ Fixation System) | OUR | 2018-06-13 | View |
No matching devices.