Hand Innovations, Inc.
FDA 510(k) & PMA Approved Devices — 10 products
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Total Devices10
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K050932 | DISTAL VOLAR RADIUS ANATOMICAL PLATE SYSTEM | LXT | 2005-04-26 | View |
| 510(k) | K042059 | SHOULDER FIXATION SYSTEM | LXT | 2004-09-30 | View |
| 510(k) | K041157 | MODIFICATION TO SMALL BONE FIXATION SYSTEM | HTY | 2004-07-30 | View |
| 510(k) | K041081 | FRAGMENT PLATE SYSTEM, SCREWS, PINS AND K-WIRES | KTT | 2004-07-01 | View |
| 510(k) | K033406 | SMALL BONE FIXATION SYSTEM | HTY | 2004-01-15 | View |
| 510(k) | K032705 | DISTAL RADIUS FRACTURE REPAIR SYSTEM | LXT | 2003-10-01 | View |
| 510(k) | K030198 | HAND INNOVATIONS, INC. DISTAL RADIUS FRACTURE REPAIR SYSTEM | HRS | 2003-04-01 | View |
| 510(k) | K023007 | DISTAL RADIUS FRACTURE REPAIR SYSTEM | HRS | 2002-12-05 | View |
| 510(k) | K013424 | INTRAMEDULLARY FIXATION SYSTEM FOR THE HAND | HTY | 2001-12-20 | View |
| 510(k) | K002775 | DISTAL VOLAR RADIUS FRACTURE REPAIR SYSTEM | HRS | 2000-12-05 | View |
No matching devices.
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