Medical Device Manufacturer · US , Draper , UT

Ortho Development - FDA 510(k) Cleared Devices

5 submissions · 5 cleared · Since 2011
5
Total
5
Cleared
0
Denied

Ortho Development has 5 FDA 510(k) cleared medical devices. Based in Draper, US.

Historical record: 5 cleared submissions from 2011 to 2014. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Ortho Development
5 devices
1-5 of 5
Cleared Jul 30, 2014
ALPINE HIP STEM
K141001 · LPH
Orthopedic · 103d
Cleared Oct 25, 2011
VUSION(R) OS
K111965 · MAX
Orthopedic · 106d
Cleared Sep 21, 2011
ORTHO DEVLOPMENT CERAMIC FEMORAL HEAD
K111936 · LZO
Orthopedic · 75d
Cleared Mar 24, 2011
BALANCED KNEE SYSTEM REVISION OFFSET TIBIA
K103837 · JWH
Orthopedic · 84d
Cleared Mar 16, 2011
ESCALADE ACETABULAR CUP SYSTEM
K103384 · LPH
Orthopedic · 118d
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