FDA 510(k) Applications Submitted by TENNILLE FOLK
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K070876 | 03/29/2007 | STRYKER TWIST DRILLS | STRYKER CRANIOMAXILLOFACIAL |
| K071628 | 06/14/2007 | STRYKER EXTERNAL FIXATION SYSTEM | STRYKER CMF |
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