Devices

Device Recall GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL

  • Modèle / numéro de série
    Lot Number 12LM03798
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    International only: Germany, France, United Arab Emirates, and United Kingdom.
  • Description du dispositif
    GENESIS(R) II CRUCIATE RETAINING ARTICULAR INSERT, TRIAL, SIZE 3-4, A/P 48 MM, M/L 68 MM, QTY 1, NON-STERILE, REF 71430490, || Product Usage: || Orthopedic
  • Manufacturer
    Smith & Nephew Inc
  • 1 Event

Fabricant

Smith & Nephew Inc
  • Adresse du fabricant
    Smith & Nephew Inc, 1450 E. Brooks Rd, Memphis TN 38116
  • Société-mère du fabricant (2017)
    Smith & Nephew plc
  • Source
    USFDA