FDA 510(k) Applications Submitted by ETEX CORP.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K090242 |
02/02/2009 |
GAMMA-BSM, BETA-BSM |
ETEX CORP. |
| K090310 |
02/06/2009 |
EQUIVABONE |
ETEX CORP. |
| K090855 |
03/30/2009 |
EQUIVABONE OSTEOINDUCTIVE BONE GRAFT SUBSTITUTE |
ETEX CORP. |
| K100883 |
03/30/2010 |
CARRIGEN |
ETEX CORP. |
| K091607 |
06/03/2009 |
ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE |
ETEX CORP. |
| K101557 |
06/04/2010 |
GAMMA-BSM, BETA-BSM, EQUIVABONE, CARIGEN |
ETEX CORP. |
| K091729 |
06/11/2009 |
ALPHA-BSM, BETA-BSM, GAMMA-BSM, EQUIVABONE |
ETEX CORP. |
| K093447 |
11/05/2009 |
CARRIGEN |
ETEX CORP. |
| K962548 |
06/28/1996 |
BSM BONE SUBSTITUTE MATERIAL KIT |
ETEX CORP. |
| K062630 |
09/05/2006 |
OSSIPRO BONE SUBSTITUTE MATERIAL |
ETEX CORP. |
| K063050 |
10/04/2006 |
CAP PLUS |
ETEX CORP. |
| K032307 |
07/25/2003 |
CAP BONE SUBSTITUTE MATERIAL |
ETEX CORP. |
| K983009 |
08/28/1998 |
BSM- BONE SUBSTITUTE MATERIAL |
ETEX CORP. |
| K080329 |
02/07/2008 |
CAP PLUS, EQUIVABONE, CAP/DBM |
ETEX CORP. |
| K072355 |
08/22/2007 |
OSSIFUSE BONE SUBSTITUTE MATERIAL |
ETEX CORP. |
| K072636 |
09/18/2007 |
A-BSM BONE SUBSTITUTE MATERIAL |
ETEX CORP. |
| K033138 |
09/30/2003 |
CAP3 BONE SUBSTITUTE MATERIAL |
ETEX CORP. |
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