FDA 510(k) Applications Submitted by CHRIS TALBOT
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K080511 |
02/25/2008 |
PLEXUR-P |
OSTEOTECH, INC. |
| K081227 |
04/30/2008 |
PLEXUR M |
OSTEOTECH, INC. |
| K082615 |
09/09/2008 |
GRAFTON R II EDBM, DEMINERALIZED BONE MATRIX ALLOGRAFT, RESORBABLE CALCIUM SALT BONE VOID FILLER DEVICES |
OSTEOTECH INC |
| K971289 |
04/07/1997 |
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM) |
OSTEOTECH, INC. |
| K991586 |
05/07/1999 |
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM) |
OSTEOTECH, INC. |
| K051188 |
05/10/2005 |
GRAFTON DBM |
OSTEOTECH, INC. |
| K051781 |
07/01/2005 |
GRAFTCAGE TLX |
OSTEOTECH, INC. |
| K042707 |
09/30/2004 |
GRAFTON PLUS DBM PASTE |
OSTEOTECH, INC. |
| K973868 |
10/10/1997 |
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM) |
OSTEOTECH, INC. |
| K053080 |
11/02/2005 |
GRAFTCAGE ACX |
OSTEOTECH, INC. |
| K043048 |
11/04/2004 |
GRAFTON PLUS DBM PASTE |
OSTEOTECH, INC. |
| K043209 |
11/19/2004 |
VIAGRAF DBM PASTE |
OSTEOTECH, INC. |
| K073405 |
12/04/2007 |
PLEXUR M |
OSTEOTECH, INC. |
| K051195 |
05/10/2005 |
GRAFTON DBM |
OSTEOTECH, INC. |
| K061982 |
07/13/2006 |
PLEXUR P |
OSTEOTECH, INC. |
| K955173 |
11/13/1995 |
SSCS (SEGMENTAL SPINAL CORRECTION SYSTEM) |
OSTEOTECH, INC. |
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