Devices

Device Recall ADVANCE DURAMER TIBIAL INSERT

  • Modèle / numéro de série
    Lot Number: 681644
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution -- United States, The Netherlands, Italy, Republic of Korea and Japan.
  • Description du dispositif
    ADVANCE DURAMER TIBIAL INSERT, REF: KIMP-312R SIZE 3 RIGHT MEDIAL PIVOT, THICKNESS 12MM, 1 EACH, STERILE EO, Wright Medical Technology, 4677 Airline Road, Arlington, TN 38002. || Indicated for use in knee arthroplasty for reduction or relief of pain and/or improved knee function in skeletally mature patients.
  • Manufacturer
    Wright Medical Technology Inc
  • 1 Event

Fabricant

Wright Medical Technology Inc
  • Adresse du fabricant
    Wright Medical Technology Inc, 5677 Airline Rd, Arlington TN 38002
  • Société-mère du fabricant (2017)
    Wright Medical Group NV
  • Source
    USFDA

Un dispositif médical avec un nom similaire

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Device Recall ADVANCE DURAMER TIBIAL INSERT
  • Modèle / numéro de série
    Lot Number: 679391
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Worldwide Distribution -- United States, The Netherlands, Italy, Republic of Korea and Japan.
  • Description du dispositif
    ADVANCE DURAMER TIBIAL INSERT, REF: KIMP-312L, SIZE 3 LEFT MEDIAL PIVOT, THICKNESS 12MM, 1 EACH, STERILE EO, Wright Medical Technology, 4677 Airline Road, Arlington, TN 38002. || Indicated for use in knee arthroplasty for reduction or relief of pain and/or improved knee function in skeletally mature patients.
  • Manufacturer
    Wright Medical Technology Inc