Linvatec Biomaterials, Ltd.
FDA 510(k) & PMA Approved Devices — 5 products
Advertisement
Total Devices5
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K042966 | DUET SUTURE ANCHOR, MODELS BXS4216, BXS4216H; IMPACT SUTURE ANCHOR, MODELS BXS4218, BXS4218H | MAI | 2004-11-19 | View |
| 510(k) | K042517 | BIOSORB FX AND BIOSORB PDX 1.5 AND 2.0 SCREWS | JEY | 2004-10-08 | View |
| 510(k) | K042295 | SMARTSCREW II, MODELS 232010, 232012, 232014, 232016, 232018, 232020 | HWC | 2004-09-16 | View |
| 510(k) | K032447 | CANNULATED NUGEN FX SCREW FULLY THREADED, CANNULATED NUGEN FX SCREW PARTIALLY THREADED | HWC | 2004-04-16 | View |
| 510(k) | K031981 | 2.4 SMARTNAIL, MODELS 532416, 532425, 532435, 532445 | MAI | 2003-07-25 | View |
No matching devices.
Advertisement