FDA 510(k) Applications Submitted by DANEK MEDICAL, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K990603 |
02/23/1999 |
MODIFICATION OF THE ZPLATE-ATL ANTERIOR FIXATION SYSTEM |
DANEK MEDICAL, INC. |
| K991528 |
05/03/1999 |
MODIFICATION TO TENOR SPINAL SYSTEM-ROD/BOLT CONNECTOR |
DANEK MEDICAL, INC. |
| K982154 |
06/19/1998 |
MODIFICATION OF TOWNLEY PEDICLE SCREW PLATING SYSTEM |
DANEK MEDICAL, INC. |
| K982875 |
08/14/1998 |
MODIFICATION TO ZPLATE-ATL ANTERIOR FIXATION SYSTEM |
DANEK MEDICAL, INC. |
| K993810 |
11/10/1999 |
CD HORIZON SPINAL SYSTEM |
DANEK MEDICAL, INC. |
| K993855 |
11/15/1999 |
ATLANTIS ANTERIOR CERVICAL PLATE SYSTEM |
DANEK MEDICAL, INC. |
| K994122 |
12/07/1999 |
BONE GRAFT WASHER, MODEL 9090114 - 9090118 |
DANEK MEDICAL, INC. |
| K984522 |
12/21/1998 |
MODIFICATION OF TSRH SPINAL SYSTEM |
DANEK MEDICAL, INC. |
| K970599 |
02/18/1997 |
TOWNLEY PEDICLE SCREW PLATING SYSTEM |
DANEK MEDICAL, INC. |
| K943827 |
08/05/1994 |
SPINE FIXATION |
DANEK MEDICAL, INC. |
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