FDA 510(k) Applications Submitted by ZIMMER CAS
| FDA 510(k) Number | Submission Date | Device Name | Applicant |
|---|---|---|---|
| K110054 | 01/07/2011 | NAVITRACK SYSTEM - OS KNEE UNIVERSAL, CAS SAME INCISION TIBIA REFERENCE | ZIMMER CAS |
| K141601 | 06/16/2014 | IASSIST KNEE SYSTEM | ZIMMER CAS |
| K131129 | 04/22/2013 | CAS PSI SHOULDER | ZIMMER CAS |
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