FDA 510(k) Applications Submitted by JOHNSON & JOHNSON COMPANY
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K060914 | 04/04/2006 | TRIDENT ANCHOR | JOHNSON & JOHNSON COMPANY |
| K063577 | 11/30/2006 | FEMORAL INTRAFIX SCREW AND SHEATH | JOHNSON & JOHNSON COMPANY |
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