FDA 510(k) Applications Submitted by GEENA AUGUSTINE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K100652 | 03/08/2010 | ACL TIGHTROPE | ARTHREX, INC. |
| K101837 | 07/01/2010 | ACL TIGHTROPE DOUBLE BUNDLE | ARTHREX, INC. |
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