FDA 510(k) Applications Submitted by PECTOFIX, INC.
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K000694 | 03/01/2000 | PECTOFIX DYNAMIC STERNAL FIXATION SYSTEM (DSF) | PECTOFIX, INC. |
| K003951 | 12/21/2000 | PECTOFIX STERNAL REPAIR WIRE | PECTOFIX, INC. |
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