Osteomed LP - FDA 510(k) Cleared Devices
29
Total
29
Cleared
0
Denied
Osteomed LP has 29 FDA 510(k) cleared medical devices. Based in Addison, US.
Historical record: 29 cleared submissions from 2003 to 2015. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Osteomed LP Filter by specialty or product code using the sidebar.
29 devices
Cleared
Apr 01, 2015
Argulated Locking Plates
Dental
132d
Cleared
Feb 24, 2014
EXTRIMILOCK ANKLE PLATING SYSTEM
Orthopedic
84d
Cleared
Jun 18, 2013
OSTEOMED EXTREMILOCK FOOT PLATING SYSTEM
Orthopedic
29d
Cleared
Jun 03, 2013
OSTEOMED SMARTFLEX CRANIAL SPRING DISTRACTOR
Neurology
167d
Cleared
Nov 29, 2012
PRIMALIF TM LLIF UNITARY PEEK LATERAL LUMBAR INTERBODY FUSION SYSTEM
Orthopedic
48d
Cleared
Apr 24, 2012
OSTEOMED WRIST PLATING SYSTEM
Orthopedic
112d
Cleared
Oct 07, 2011
OSTEOMED HAND FUSION SYSTEM
Orthopedic
140d
Cleared
Aug 15, 2011
OSTEOMED LOW PROFILE NEURO FIXATION SYSTEM
Neurology
110d
Cleared
Sep 30, 2010
PRIMALOK FACET FIXATION SYSTEM
Orthopedic
35d
Cleared
Aug 17, 2010
PRIMAL OK INTERSPINOUS FUSION SYSTEM
Orthopedic
186d
Cleared
Sep 10, 2009
OSTEOMED FOOT PLATING SYSTEM
Orthopedic
99d
Cleared
Jul 02, 2009
OSTEOMED HAND PLATE AND SCREW FIXATION SYSTEM
Orthopedic
126d