Medical Device Manufacturer · US , Allendale, , NJ

Howmedica Osteonics - FDA 510(k) Cleared Devices

13 submissions · 13 cleared · Since 2001
13
Total
13
Cleared
0
Denied

Howmedica Osteonics has 13 FDA 510(k) cleared orthopedic devices. Based in Allendale,, US.

Historical record: 13 cleared submissions from 2001 to 2012.

Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.

FDA 510(k) Regulatory Record - Howmedica Osteonics
13 devices
1-13 of 13
Cleared Mar 29, 2012
ACCOLADE II HIP STEM
K120578 · JDI
Orthopedic · 31d
Cleared Mar 03, 2011
RESTORATION ACETABULAR WEDGE AUGMENTS
K102019 · LPH
Orthopedic · 227d
Cleared Jan 22, 2007
TRIATHLON CS (CONDYLAR STABILIZING) LIPPED INSERT
K063423 · JWH
Orthopedic · 70d
Cleared Mar 09, 2004
BONESAVE BONE VOID FILLER
K033258 · MQV
Orthopedic · 152d
Cleared Dec 10, 2003
STRYKER SPINE MAPS SYSTEM
K032855 · MNH
Orthopedic · 89d
Cleared Aug 08, 2003
REFLEX ANTERIOR CERVICAL PLATE SYSTEM
K031702 · KWQ
Orthopedic · 67d
Cleared Aug 04, 2003
BONESOURCE BVF
K031435 · MQV
Orthopedic · 90d
Cleared May 23, 2003
GMRS PRESS FIT STEMS WITH PUREFIX HA
K031217 · LZO
Orthopedic · 36d
Cleared Aug 22, 2002
S2 FEMORAL NAIL
K022461 · HSB
Orthopedic · 27d
Cleared Aug 01, 2002
XIA SPINAL SYSTEM
K022160 · MNI
Orthopedic · 29d
Cleared Dec 03, 2001
MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM
K013772 · LXT
Orthopedic · 20d
Cleared Oct 10, 2001
DURACON PS LIPPED TIBIAL INSERT
K012172 · JWH
Orthopedic · 90d
Cleared Jul 20, 2001
MODIFICATION TO XIA SPINE SYSTEM
K012027 · MNH
Orthopedic · 22d
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