Device Recall PopLok Punch

  • Model / Serial
    Lot 318455
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution -- US and Korea.
  • Product Description
    PopLok Punch labeled in part: || "PKL-35M***3.5mm***QTY 1***PopLok Punch***ConMed Linvatec Biomaterials, Ltd. Hermiankatu 6-8L 33720 Tampere, FINLAND***Rx Only***ConMed Linvatec 11311 Concept Blvd Largo, FL 33773-4908 USA***Made in USA***" || Intended Use: Bone Punch.
  • Manufacturer
  • 1 Event

Manufacturer

  • Manufacturer Address
    Linvatec Corp. dba ConMed Linvatec, 11311 Concept Blvd, Largo FL 33773-4908
  • Manufacturer Parent Company (2017)
  • Source
    USFDA

One device with a similar name

Learn more about the data here

  • Model / Serial
    Lot 256058
  • Product Classification
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Worldwide Distribution - USA including California and Internationally to Spain and Korea
  • Product Description
    ConMed Linvatec Biomaterials, PopLok bone Punch PKL-35M, 3.5mm || Orthopedic manual surgical instrument - Bone Punch
  • Manufacturer