FDA 510(k) Applications Submitted by STRYKER CMF
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K071628 | 06/14/2007 | STRYKER EXTERNAL FIXATION SYSTEM | STRYKER CMF |
| K060750 | 03/21/2006 | STRYKER INJECTABLE CEMENT | STRYKER CMF |
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