FDA 510(k) Applications Submitted by KARL VON BERGE
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K093533 | 11/16/2009 | ZIMMER PATIENT SPECIFIC INSTRUMENTS SYSTEM, VERSION 2.0 | MATERIALISE N.V. |
| K091263 | 04/30/2009 | ZIMMER PATIENT SPECIFIC INSTRUMENTS, ZIMMER PATIENT SPECIFIC INSTRUMENTS PLANNER, MODEL 1.1 (4.3.0.35) | MATERIALISE N.V. |
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