Medical Device Manufacturer · US , Walker , MI

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

8 submissions · 8 cleared · Since 1984

8

Total

8

Cleared

0

Denied

Orthomatrix, Inc. has 8 FDA 510(k) cleared medical devices. Based in Walker, US.

Historical record: 8 cleared submissions from 1984 to 2001. Primary specialty: Orthopedic.

Browse the FDA 510(k) cleared devices submitted by Orthomatrix, Inc. Filter by specialty or product code using the sidebar.

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

8 devices

1-8 of 8

Cleared Aug 01, 2001

CANNULATED PLUS SCREW SYSTEM

Orthopedic · 142d

Cleared Dec 13, 2000

ORTHOMATRIX, INC. CERCLAGE SYSTEM

Orthopedic · 238d

Cleared Mar 10, 2000

MAGELLAN TIBIAL INTRAMEDULLARY NAIL

Orthopedic · 199d

Cleared Mar 10, 2000

MAGELLAN HUMERAL INTRAMEDULLARY NAIL

Orthopedic · 199d

Cleared Oct 21, 1985

HA-1000 & HA-500 HYDROXYLAPATITE TOOTH ROOT SUBSTI

Cleared Sep 23, 1985

HA-2000 HYDROXYLAPATITE

Cleared May 21, 1985

HA-1000 & HA-500 HYDROXYLAPATITE-MODIFICATION

Chemistry · 46d

Cleared Aug 09, 1984

RIDGEMATRIX 20/40 MESH, PERIOMATRIX