Devices

Device Recall T2 Ankle Arthrodesis Nail

  • Modèle / numéro de série
    lot codes: K108843, K152964, K171685, K180561, K194187, K227390, K253168, K733141, K776745, K785626, K785652, K802766, K831465, K837694, K868868, and  K999298.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Stryker T2 Ankle Arthrodesis Nail, right; 012 x 300 mm; Catalog number: 18191230S; || Sterile, TI Alloy; || Stryker Trauma GmbH, Germany; || Distributed in the US by Howmedica Osteonics Corp, Mahwah, NJ. || Intended for tibiotalocalcaneal arthrodesis (fusion) and to provide stabilization of the hindfoot and ankle including the transverse tarsal joints coupling the mid-foot to the hindfoot.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
  • 1 Event

Fabricant

Stryker Howmedica Osteonics Corp.
  • Adresse du fabricant
    Stryker Howmedica Osteonics Corp., 325 Corporate Drive, Mahwah NJ 07430
  • Société-mère du fabricant (2017)
    Stryker
  • Source
    USFDA

5 dispositifs médicaux avec un nom similaire

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Device Recall T2 Ankle Arthrodesis Nail Surgical Protocol
  • Modèle / numéro de série
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution
  • Description du dispositif
    T2 Ankle Arthrodesis Nail Surgical Protocol, Catalog Number LT2AA-OT, Stryker Orthopaedics || The Surgical Protocol instructs surgeons on proper surgical technique for the T2 Ankle Arthrodesis Nail.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall T2 Ankle Arthrodesis Nail
  • Modèle / numéro de série
    lot codes: K152966, K177319, K208221, K230272, K254574, K735537, K779942, K841062, K842726, K868798, K868816, K883947, and  K892961.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Stryker T2 Ankle Arthrodesis Nail, left; 011 x 300 mm; Catalog Number: 18181130S; || Sterile, TI Alloy; || Stryker Trauma GmbH, Germany; || Distributed in the US by Howmedica Osteonics Corp, Mahwah, NJ. || Intended for tibiotalocalcaneal arthrodesis (fusion) and to provide stabilization of the hindfoot and ankle including the transverse tarsal joints coupling the mid-foot to the hindfoot.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall T2 Ankle Arthrodesis Nail
  • Modèle / numéro de série
    lot codes: K163646, K192333, K236971, K472870, K733121, K776754, K785625, K842732, K868822, K875207, K893039, and  K977374.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Stryker T2 Ankle Arthrodesis Nail, left; 012 x 300 mm; Catalog number: 18181230S; || Sterile, TI Alloy; || Stryker Trauma GmbH, Germany; || Distributed in the US by Howmedica Osteonics Corp, Mahwah, NJ. || Intended for tibiotalocalcaneal arthrodesis (fusion) and to provide stabilization of the hindfoot and ankle including the transverse tarsal joints coupling the mid-foot to the hindfoot.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall T2 Ankle Arthrodesis Nail
  • Modèle / numéro de série
    lot codes: K101051, K157119, K185536, K210257, K549634, K735538, K769105, K779949, K837690, K868843, and  K893064.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Stryker T2 Ankle Arthrodesis Nail, right; 010 x 300 mm; Catalog number: 18191030S; || Sterile, TI Alloy; || Stryker Trauma GmbH, Germany; || Distributed in the US by Howmedica Osteonics Corp, Mahwah, NJ. || Intended for tibiotalocalcaneal arthrodesis (fusion) and to provide stabilization of the hindfoot and ankle including the transverse tarsal joints coupling the mid-foot to the hindfoot.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall T2 Ankle Arthrodesis Nail
  • Modèle / numéro de série
    lot codes: K125357, K158792, K185537, K199852, K227392, K452805, K455652, K461353, K624000, K732800, K769107, K782950, K785627, K820525, K858019, K863219, K868858, K893086, K951620, K963944, and  K983458.
  • Classification du dispositif
    Orthopedic Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    Yes
  • Distribution
    Nationwide Distribution.
  • Description du dispositif
    Stryker T2 Ankle Arthrodesis Nail, right; 011 x 300 mm; Catalog number: 18191130S; || Sterile, TI Alloy; || Stryker Trauma GmbH, Germany; || Distributed in the US by Howmedica Osteonics Corp, Mahwah, NJ. || Intended for tibiotalocalcaneal arthrodesis (fusion) and to provide stabilization of the hindfoot and ankle including the transverse tarsal joints coupling the mid-foot to the hindfoot.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.