FDA 510(k) Applications Submitted by ALYSSA THOMAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K061206 | 05/01/2006 | ACUTE BONE SCREW | ACUTE INNOVATIONS LLC |
| K081588 | 06/05/2008 | RE-ZORB PLATING SYSTEM | ACUTE INNOVATIONS LLC |
| K083144 | 10/23/2008 | ACUMED CLAVICLE SCREW SYSTEM | ACUMED LLC |
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