Devices

ProVision Hytrel Elastomer Hood; product 5431-05-000.

  • Modèle / numéro de série
    All product manufactured between February 1, 2002 and June 17, 2003 that does not have a green square on the label above the CE mark. Product bearing the green square on the label has been 100% inspected and is not under recall.
  • Classification du dispositif
    General Hospital and Personal Use Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    United States, Australia, Canada, Chile, England, India, Japan, Malaysia, Singapore, South Africa, Taiwan and United Kingdom
  • Description du dispositif
    ProVision Hytrel Elastomer Hood; product 5431-05-000.
  • Manufacturer
    Depuy Orthopaedics, Inc.
  • 1 Event

Fabricant

Depuy Orthopaedics, Inc.
  • Adresse du fabricant
    Depuy Orthopaedics, Inc., 700 Orthopaedic Drive, Warsaw IN 46581
  • Source
    USFDA