FDA 510(k) Applications Submitted by OSTEOMEDICS, INC.
| FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
| K010118 |
01/16/2001 |
NORMED MANDIBULAR FIXATION SYSTEM |
OSTEOMEDICS, INC. |
| K021341 |
04/29/2002 |
NORMED BONE TRANSPORT DISTRACTION DEVICE |
OSTEOMEDICS, INC. |
| K021342 |
04/29/2002 |
NORMED BI-DIRECTIONAL/MULTIDIRECTIONAL JAW DISTRACTOR |
OSTEOMEDICS, INC. |
| K022230 |
07/10/2002 |
NORMED MINI EXTERNAL FIXATOR SYSTEM |
OSTEOMEDICS, INC. |
| K022231 |
07/10/2002 |
NORMED DISTAL RADIUS RECONSTRUCTION SYSTEM |
OSTEOMEDICS, INC. |
| K022323 |
07/17/2002 |
NORMED TITANIUM RONDO FIX FUSION PLATES AND SCREW SYSTEM |
OSTEOMEDICS, INC. |
| K022324 |
07/17/2002 |
NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM |
OSTEOMEDICS, INC. |
| K022325 |
07/17/2002 |
NORMED TITANIUM OSTEOTOMY PLATING SYSTEM |
OSTEOMEDICS, INC. |
| K022035 |
06/21/2002 |
OSTEOMEDICS RESORBABLE SMALL FIXATION SYSTEM, OSTEOSORB |
OSTEOMEDICS, INC. |
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