Device Recall Reflex Revision Screwdriver Inner Shaft

  • Modèle / numéro de série
    Lot codes: 26719, 047377, 047570, 065167, 06A167, and 072689.
  • Classification du dispositif
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    The product was distributed to 13 Stryker branches/agencies.
  • Description du dispositif
    Reflex Revision Screwdriver Inner Shaft is a orthopedic manual surgical instrument that is a nonpowered, hand held device intended for medical purposes to manipulate tissue, or for use with other devices in orthopedic surgery. Ref Number 48500900;Non Sterile
  • Manufacturer
  • 1 Event

Fabricant

  • Adresse du fabricant
    Stryker Spine, 2 Pearl Ct, Allendale NJ 07401-1611
  • Société-mère du fabricant (2017)
  • Source
    USFDA