Manufacturers

Sulzer Spine-Tech

  • Adresse du fabricant
    Sulzer Spine-Tech, 7375 Bush Lake Road, Minneapolis MN 55439-2027
  • Source
    USFDA
  • 1 Event

Un dispositif médical dans la base de données

Device Recall SpineTech
  • Modèle / numéro de série
    Lot numbers P010900 and P010957
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    1
  • Dispositif implanté ?
    No
  • Distribution
    The instruments to be recalled are at 2 consignees in California and Mississippi. 21 units are with the firm''s sales representatives.
  • Description du dispositif
    Spine-Tech Ancillary Discectomy Instrument (Box Curette), Catalog Number 07.00254.001, in Spine-Tech Ancillary Discectomy Instrument Set, Catalog Number 07.00316.001.