Medical Device Manufacturer · US , Walker , MI

Orthomatrix, Inc. - FDA 510(k) Cleared Devices

8 submissions · 8 cleared · Since 1984

Recent clearances: CANNULATED PLUS SCREW SYSTEM, ORTHOMATRIX, INC. CERCLAGE SYSTEM, MAGELLAN TIBIAL INTRAMEDULLARY NAIL

View 8 510(k) Devices ↓

8

Total

8

Cleared

0

Denied

FDA 510(k) Regulatory Record - Orthomatrix, Inc. Chemistry ✕

1 devices

1-1 of 1

Cleared May 21, 1985

HA-1000 & HA-500 HYDROXYLAPATITE-MODIFICATION

Chemistry · 46d