Device Recall Reflex Revision Screwdriver Inner Shaft

  • Modelo / Serial
    Lot codes: 26719, 047377, 047570, 065167, 06A167, and 072689.
  • Clasificación del producto
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    The product was distributed to 13 Stryker branches/agencies.
  • Descripción del producto
    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

Fabricante

  • Dirección del fabricante
    Stryker Spine, 2 Pearl Ct, Allendale NJ 07401-1611
  • Empresa matriz del fabricante (2017)
  • Source
    USFDA