Medical Device Manufacturer · US , Washington , DC

Corin Orthopedic Products - FDA 510(k) Cleared Devices

5 submissions · 3 cleared · Since 1993
5
Total
3
Cleared
0
Denied

Corin Orthopedic Products has 3 FDA 510(k) cleared medical devices. Based in Washington, US.

Historical record: 3 cleared submissions from 1993 to 1994. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Corin Orthopedic Products Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Corin Orthopedic Products
5 devices
1-5 of 5
Cleared Oct 07, 1994
CORIN AUSTIN-MOORE PROSTHESIS, MODIFICATION
K931752 · KWL
Orthopedic · 547d
Cleared Oct 07, 1994
CORIN THOMPSON PROSTHESIS, MODIFICATION
K931753 · KWL
Orthopedic · 547d
Cleared Sep 07, 1994
NUFFIELD TOTAL KNEE UHMWPE TIBIA (ONE PIECE) MODIFICATION
K934166 · JWH
Orthopedic · 376d
Cleared Sep 23, 1993
CENATOR TOTAL HIP SYSTEM
K925866 · JDI
Orthopedic · 308d
Cleared Aug 09, 1993
CORIN BIPOLAR PROSTHESIS
K925897 · KWY
Orthopedic · 263d
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