Devices

Device Recall SpineTech

  • Modelo / Serial
    Lot numbers P010900 and P010957
  • Clasificación del producto
    Orthopedic Devices
  • Clase de dispositivo
    1
  • ¿Implante?
    No
  • Distribución
    The instruments to be recalled are at 2 consignees in California and Mississippi. 21 units are with the firm''s sales representatives.
  • Descripción del producto
    Spine-Tech Ancillary Discectomy Instrument (Box Curette), Catalog Number 07.00254.001, in Spine-Tech Ancillary Discectomy Instrument Set, Catalog Number 07.00316.001.
  • Manufacturer
    Sulzer Spine-Tech
  • 1 Event

Fabricante

Sulzer Spine-Tech
  • Dirección del fabricante
    Sulzer Spine-Tech, 7375 Bush Lake Road, Minneapolis MN 55439-2027
  • Source
    USFDA