FDA 510(k) Applications Submitted by STUCKENBROCK MEDIZINTECHNIK GMBH
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K042902 | 10/20/2004 | HERBERT ULNAR HEAD PROSTHESIS SYSTEM | STUCKENBROCK MEDIZINTECHNIK GMBH |
| K171624 | 06/02/2017 | IXOS Radius Plate System | Stuckenbrock Medizintechnik GmbH |
| K171628 | 06/02/2017 | HBS2 Headless Bone Screw | Stuckenbrock Medizintechnik GmbH |
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