FDA 510(k) Applications Submitted by SYNTHES (USA) PRODUCTS LLC/NORIAN CORPORATION
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K113079 | 10/17/2011 | SYNTHES HEMOSTATIC BONE PUTTY | SYNTHES (USA) PRODUCTS LLC/NORIAN CORPORATION |
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