Device Recall Optetrak

  • 모델명 / 제조번호(시리얼번호)
    serial numbers: 0900529-0900532
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    Distributed to one hospital in New York.
  • 제품 설명
    Polyethylene tibial posterior stabilized components. Optetrak All Poly Tibial PS Component. Knee prosthesis. Catalog number : 204-11-13
  • Manufacturer
  • 1 Event

제조사

  • 제조사 주소
    Exactech, Inc., 2320 NW 66th Ct, Gainesville FL 32653-1630
  • 제조사 모회사 (2017)
  • Source
    USFDA

유사한 이름을 가진 의료기기 1건 유사한 이름을 가진 의료기기 3 건

데이터에 대해 더 자세히 알아보기 여기

  • 모델명 / 제조번호(시리얼번호)
    Catalogue number 200-04-45; Serial number range 0730621-07306351; Lot number 452500.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    Distributed domestically to Alabama and Louisiana, and internationally to Spain, Germany and Greece.
  • 제품 설명
    Product is Optetrak Cemented Finned Tibial Tray Sz. 4F/5T. Knee prosthesis. Product is labeled in part: ''OPTETRAK FINNED TIBIAL TRAY A/P53 mm M/L 83mm***STERILE, SINGLE USE ONLY FOR CEMENTED USE ONLY***EXACTECH Gainesville, FL 32653***. ''
  • Manufacturer
  • 모델명 / 제조번호(시리얼번호)
    Serial numbers 0886395-0886424
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    International distribution only---- including countries of South America, Africa and Europe
  • 제품 설명
    Optetrak, B-series cemented finned tibial tray size 2f/2t. Catalog # 220-04-02
  • Manufacturer
  • 모델명 / 제조번호(시리얼번호)
    Catalog numbers 02-012-35-6011, 02-012-35-6013, 02-012-35-6015 All lots.
  • 의료기기 분류등급
  • 의료기기 등급
    2
  • 이식된 장치?
    Yes
  • 유통
    USA ( nationwide) WA, OH, OK, TX, NC, NY, CO, VA, MA, IL, TN, MN, NJ and FL.
  • 제품 설명
    OPTETRAK LOGIC TIBIAL INSERT POSTERIOR STABILIZED***Match Component Colors 6 YELLOW, 11mm, Use with LOGIC Femoral and Tibial Components***REF 02-012-35-6011. || There are three product sizes being recalled, 11mm, 13mm, 15mm. All other information is the same. || The Optetrak Logic Total Knee System is indicated for use in skeletally mature individuals undergoing primary surgery for total knee replacement due to osteoarthritis, osteonecrosis, rheumatoid arthritis, and/or post-traumatic degenerative problems. They are also indicated for revision of failed previous reconstructions where sufficient bone stock and soft tissue integrity are present.
  • Manufacturer