Howmedica Osteonics is one of 19908 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Howmedica Osteonics - FDA 510(k) Cleared Devices
Recent clearances: ACCOLADE II HIP STEM, RESTORATION ACETABULAR WEDGE AUGMENTS, TRIATHLON CS (CONDYLAR STABILIZING) LIPPED INSERT
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
Cleared
Mar 29, 2012
ACCOLADE II HIP STEM
Orthopedic
31d
Cleared
Mar 03, 2011
RESTORATION ACETABULAR WEDGE AUGMENTS
Orthopedic
227d
Cleared
Jan 22, 2007
TRIATHLON CS (CONDYLAR STABILIZING) LIPPED INSERT
Orthopedic
70d
Cleared
Mar 09, 2004
BONESAVE BONE VOID FILLER
Orthopedic
152d
Cleared
Dec 10, 2003
STRYKER SPINE MAPS SYSTEM
Orthopedic
89d
Cleared
Aug 08, 2003
REFLEX ANTERIOR CERVICAL PLATE SYSTEM
Orthopedic
67d
Cleared
Aug 04, 2003
BONESOURCE BVF
Orthopedic
90d
Cleared
May 23, 2003
GMRS PRESS FIT STEMS WITH PUREFIX HA
Orthopedic
36d
Cleared
Aug 22, 2002
S2 FEMORAL NAIL
Orthopedic
27d
Cleared
Aug 01, 2002
XIA SPINAL SYSTEM
Orthopedic
29d
Cleared
Dec 03, 2001
MODIFICATION TO HOFFMANN II MICRO EXTERNAL FIXATION SYSTEM
Orthopedic
20d
Cleared
Oct 10, 2001
DURACON PS LIPPED TIBIAL INSERT
Orthopedic
90d
Cleared
Jul 20, 2001
MODIFICATION TO XIA SPINE SYSTEM
Orthopedic
22d