Medical Device Manufacturer · CA , Montreal

Zimmer Cas - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 2011
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Zimmer Cas Orthopedic ✕

3 devices
1-3 of 3
Cleared Sep 11, 2014
IASSIST KNEE SYSTEM
K141601 · OLO
Orthopedic · 87d
Cleared Aug 20, 2013
CAS PSI SHOULDER
K131129 · KWS
Orthopedic · 120d
Cleared Mar 24, 2011
NAVITRACK SYSTEM - OS KNEE UNIVERSAL, CAS SAME INCISION TIBIA REFERENCE
K110054 · OLO
Orthopedic · 76d
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