Etex Corp.
FDA 510(k) & PMA Approved Devices — 18 products
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Total Devices18
Categories0
Latest FDA decision
| Type | Number | Device Name | Code | Date | Actions |
|---|---|---|---|---|---|
| 510(k) | K100883 | CARRIGEN | LYC | 2010-12-21 | View |
| 510(k) | K101557 | GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN | MQV | 2010-07-01 | View |
| 510(k) | K093447 | CARRIGEN | MQV | 2010-02-18 | View |
| 510(k) | K091729 | ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE | LYC | 2009-12-23 | View |
| 510(k) | K091607 | ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE | MQV | 2009-11-02 | View |
| 510(k) | K090855 | EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE | MQV | 2009-09-18 | View |
| 510(k) | K090310 | EQUIVABONE | MQV | 2009-03-24 | View |
| 510(k) | K090242 | GAMMA-BSM, BETA-BSM | MQV | 2009-02-20 | View |
| 510(k) | K080329 | CAP PLUS, EQUIVABONE, CAP/DBM | MBP | 2008-04-28 | View |
| 510(k) | K063050 | CAP PLUS | MQV | 2007-11-19 | View |
| 510(k) | K072636 | A-BSM BONE SUBSTITUTE MATERIAL | MQV | 2007-10-23 | View |
| 510(k) | K072355 | OSSIFUSE BONE SUBSTITUTE MATERIAL | MQV | 2007-09-26 | View |
| 510(k) | K062630 | OSSIPRO BONE SUBSTITUTE MATERIAL | MQV | 2007-06-28 | View |
| 510(k) | K033138 | CAP3 BONE SUBSTITUTE MATERIAL | MQV | 2003-12-02 | View |
| 510(k) | K032307 | CAP BONE SUBSTITUTE MATERIAL | GXP | 2003-10-24 | View |
| 510(k) | K983009 | BSM- BONE SUBSTITUTE MATERIAL | GXP | 1998-11-25 | View |
| 510(k) | K962548 | BSM BONE SUBSTITUTE MATERIAL KIT | LYC | 1997-08-05 | View |
| 510(k) | K935696 | ETEX HA HIP REPLACEMENT SYSTEM | MEH | 1994-07-22 | View |
No matching devices.
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