Medical Device Manufacturer · US , Paramus , NJ

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

9 submissions · 9 cleared · Since 2001
9
Total
9
Cleared
0
Denied

Osteomedics, Inc. has 9 FDA 510(k) cleared medical devices. Based in Paramus, US.

Historical record: 9 cleared submissions from 2001 to 2003. Primary specialty: Orthopedic.

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

FDA 510(k) Regulatory Record - Osteomedics, Inc.
9 devices
1-9 of 9
Cleared Jan 17, 2003
OSTEOMEDICS RESORBABLE SMALL FIXATION SYSTEM, OSTEOSORB
K022035 · JEY
Dental · 210d
Cleared Sep 17, 2002
NORMED TITANIUM CALCANEUS PLATING WITH LOCKING SCREW SYSTEM
K022324 · HRS
Orthopedic · 62d
Cleared Sep 13, 2002
NORMED DISTAL RADIUS RECONSTRUCTION SYSTEM
K022231 · HRS
Orthopedic · 65d
Cleared Sep 10, 2002
NORMED MINI EXTERNAL FIXATOR SYSTEM
K022230 · HRS
Orthopedic · 62d
Cleared Sep 09, 2002
NORMED TITANIUM RONDO FIX FUSION PLATES AND SCREW SYSTEM
K022323 · HRS
Orthopedic · 54d
Cleared Sep 09, 2002
NORMED TITANIUM OSTEOTOMY PLATING SYSTEM
K022325 · HRS
Orthopedic · 54d
Cleared Aug 01, 2002
NORMED BONE TRANSPORT DISTRACTION DEVICE
K021341 · JEY
Dental · 94d
Cleared Aug 01, 2002
NORMED BI-DIRECTIONAL/MULTIDIRECTIONAL JAW DISTRACTOR
K021342 · JEY
Dental · 94d
Cleared Aug 14, 2001
NORMED MANDIBULAR FIXATION SYSTEM
K010118 · JEY
Dental · 210d
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