Medical Device Manufacturer · US , Warsaw , IN

Depuy France - FDA 510(k) Cleared Devices

2 submissions · 2 cleared · Since 2012
2
Total
2
Cleared
0
Denied

Depuy France has 2 FDA 510(k) cleared medical devices. Based in Warsaw, US.

Historical record: 2 cleared submissions from 2012 to 2012. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Depuy France Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Depuy France
2 devices
1-2 of 2
Cleared Sep 06, 2012
DEPUY CTA REVERSE SHOULDER SYSTEM
K122442 · PHX
Orthopedic · 27d
Cleared Jun 11, 2012
DEPUT DELTA XTEND REVERSE SHOULDER
K120174 · PHX
Orthopedic · 143d
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