Osteonics(R) Omnifit(R) Normalized Hip Stem

• • Terminated Z-0892-2009 FDA Unclassified (pre-2012) ·initiated 13 Nov 2008

  Stryker Orthopaedics became aware of a visual defect in certain blister packages of certain devices.

510(k) Number

K932519 ↗

FDA Product Code

LZO

Device Class

Class II

Regulation

21 CFR Part 888.3353

Advisory Committee

Orthopedic

FDA Decision

SN

• Omnifit II Hip Prostheses: Cement Fixation

  Class II

  FDA 510(k) K870235 Active Cleared 29 May 1987

• Osteonics Total Elbow System Open recall

  Class II

  FDA 510(k) K980502 Active Cleared 5 May 1998

• MC2P Acetabular Component Open recall

  Class II

  FDA 510(k) K900438 Active Cleared 18 Apr 1990

• Shoulder Microstructured Humeral Prosthesis

  Class II

  FDA 510(k) K883816 Active Cleared 10 Nov 1988

• Osteonics(R) Mpss Hip Stem Series

  Class II

  FDA 510(k) K905275 Active Cleared 28 Jan 1991

• Osteonics 7000 Series Total Knee Tibial Components

  Class II

  FDA 510(k) K910990 Active Cleared 19 Jun 1991

See all devices from Osteonics Corp. →