Devices

Device Recall SpineTech

  • 모델명 / 제조번호(시리얼번호)
    Lot numbers P010900 and P010957
  • 의료기기 분류등급
    Orthopedic Devices
  • 의료기기 등급
    1
  • 이식된 장치?
    No
  • 유통
    The instruments to be recalled are at 2 consignees in California and Mississippi. 21 units are with the firm''s sales representatives.
  • 제품 설명
    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

제조사

Sulzer Spine-Tech
  • 제조사 주소
    Sulzer Spine-Tech, 7375 Bush Lake Road, Minneapolis MN 55439-2027
  • Source
    USFDA