Bioretec, Ltd.
FDA 510(k) & PMA Approved Devices — 8 products
Advertisement
Total Devices8
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K261057 | ActivaScrew™ Cannulated COM | HWC | 2026-09-04 | View |
| 510(k) | K130716 | BIORETEC ACTIVASCREW INTERFERENCE | MAI | 2013-08-28 | View |
| 510(k) | K080879 | ACTIVATM PRODUCT GROUP INCLUDING BIOABSORBABLE DEVICES ACTIVAPIN FUSION, ACTIVANAILTM CONICALTM | HTY | 2008-06-24 | View |
| 510(k) | K081392 | BIORETEC ACTIVASCREW, ACTIVASCREW CANNULATED AND ACTIVASCREW CANNULATED WITH ACTIVAPIN | HWC | 2008-06-18 | View |
| 510(k) | K072848 | ACTIVASCREW | HWC | 2007-11-02 | View |
| 510(k) | K071863 | ACTIVAPIN, NEXFIX RFS PIN, NEXFIX RESORBABLE FIXATION SYSTEM (RFS) | HTY | 2007-08-31 | View |
| 510(k) | K062980 | ACTIVASCREW | HWC | 2006-11-22 | View |
| 510(k) | K061164 | ACTIVAPIN | HTY | 2006-07-06 | View |
No matching devices.
Advertisement