Medical Device Manufacturer · US , Warsaw , IN

Zimmer - FDA 510(k) Cleared Devices

3 submissions · 3 cleared · Since 1984
Official Website
3
Total
3
Cleared
0
Denied

FDA 510(k) Regulatory Record - Zimmer Orthopedic ✕

3 devices
1-3 of 3
Cleared Jun 16, 2015
Zimmer PSI Shoulder System
K150730 · KWT
Orthopedic · 88d
Cleared Nov 30, 2012
SMARTTOOLS KNEE SYSTEM
K122326 · OLO
Orthopedic · 121d
Cleared Jan 30, 1984
BIPOLAR HIP DEVICE
K833991 · KWY
Orthopedic · 70d
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