FDA 510(k) Applications Submitted by MELISSA EGAN
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K112526 | 08/31/2011 | TWINFIX ULTRA TI, TWINFIX ULTRA PK, TWINFIX ULTRA HA SUTURE ANCHORS | SMITH & NEPHEW, INC. |
| K113274 | 11/07/2011 | FOOTPRINT ULTRA PK SUTURE ANCHOR | SMITH & NEPHEW, INC. |
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