FDA 510(k) Applications Submitted by NOVIACE CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K030989 | 03/28/2003 | OSTEOSORB TACK FIXATION SYSTEM | NOVIACE CORPORATION |
| K032634 | 08/26/2003 | NORMED COMPRESSION BONE SCREW SYSTEM | NOVIACE CORPORATION |
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