Howmedica Osteonics Corp. - FDA 510(k) Cleared Devices
288
Total
288
Cleared
0
Denied
Howmedica Osteonics Corp. has 288 FDA 510(k) cleared orthopedic devices. Based in Allendale, US.
Historical record: 288 cleared submissions from 1999 to 2020.
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) cleared devices by Howmedica Osteonics Corp.
288 devices
Cleared
Aug 13, 2020
Exeter V40 Femoral Stem, Exeter X3 RimFit Cup
Orthopedic
247d
Cleared
May 13, 2020
Triathlon Posterior Stabilized Femoral Component - beaded with Peri-Apatite,...
Orthopedic
48d
Cleared
Dec 27, 2013
REUNION RSA SHOULDER SYSTEM
Orthopedic
270d
Cleared
Aug 16, 2013
ABG III MONOLITHIC HIP STEM
Orthopedic
268d
Cleared
Feb 22, 2013
DISTAL FEMORAL GROWING PROSTHESIS, TIBIAL ROTATING COMPONENTS, BEARING, AXIS,...
Orthopedic
227d
Cleared
Feb 14, 2013
TRIATHLON ALL-POLYETHYLENE CONDYLAR STABILIZING (CS) TIBIAL IMPLANTS...
Orthopedic
128d
Cleared
Feb 01, 2013
NOVEL FIT AND FILL STEM
Orthopedic
136d
Cleared
Nov 01, 2012
STRYKER CMF MEDPOR CUSTOMIZED IMPLANT
General & Plastic Surgery
183d
Cleared
Jul 30, 2012
HIP SYSTEMS
Orthopedic
90d
Cleared
Feb 15, 2012
S2 FEMORAL A/R NAIL S2 FEMORAL COMRESSION NAIL S2 TIBIAL NAIL S2 TIBIAL...
Orthopedic
89d
Cleared
Sep 28, 2011
ADM AND ADM/MDM DURATION INSERTS, ADM AND ADM/MDM X3 INSERTS
Orthopedic
26d
Cleared
Sep 27, 2011
EXETER HIP STEM
Orthopedic
238d
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