Devices

Device Recall DePuy Orthopedics

Manufacturer

Depuy Orthopaedics, Inc.
  • Manufacturer Address
    Depuy Orthopaedics, Inc., 700 Orthopaedic Dr, Warsaw IN 46582-3994
  • Source
    USFDA

2 devices with a similar name

Learn more about the data here

Device Recall DePuy Orthopedics
  • Model / Serial
    Lot Umber: 330722
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    IA
  • Product Description
    P.F.C.¿ Modular Knee System || Modular Plus Tibial Wedge || 10¿ HEMI x 8.5MM HEIGHT || Product Code: 86-0178
  • Manufacturer
    Depuy Orthopaedics, Inc.
Device Recall DePuy Orthopedics
  • Model / Serial
    Lot Number: 226436R
  • Product Classification
    Orthopedic Devices
  • Device Class
    2
  • Implanted device?
    Yes
  • Distribution
    NY
  • Product Description
    P.F.C. ¿ ¿ Knee System 7¿ || Fluted Femoral Stem 18mmX125mm || REF 96-1703
  • Manufacturer
    Depuy Orthopaedics, Inc.