Devices

Anterior Cervical Fusion Pack

  • Modèle / numéro de série
    Lot Numbers; Expiration Dates:  62090 11/18/2015 64503 11/20/2015 65165 11/9/2015 66042 7/15/2016 68496 9/18/2016 75702 7/4/2017 76407 2/4/2017 78060 2/23/2017 78683 9/8/2017 79143 11/3/2017
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
  • Description du dispositif
    Anterior Cervical Fusion Pack, Kit part numbers: AMS2502 and AMS2502(A || convenience custom kits used for general surgery in hospital operating room
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Fabricant

Windstone Medical Packaging, Inc.
  • Adresse du fabricant
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Société-mère du fabricant (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA

Un dispositif médical avec un nom similaire

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Device Recall Anterior Cervical Fusion Pack
  • Modèle / numéro de série
    Lot numbers and Expiration dates:  84343, 5/20/2018 88052, 11/11/2018 89579, 11/15/2018 89709, 12/10/2018 94934, 1/4/2019 95441, 6/3/2019
  • Classification du dispositif
    General and Plastic Surgery Devices
  • Classe de dispositif
    2
  • Dispositif implanté ?
    No
  • Distribution
    Distributed in AZ, CA, CO, CT, FL, GA, IL, IN, KS, LA, MA, MD, MI, MN, MO, NC, ND, NE, NJ, NV, OH, PA, TX, UT, VA, and WA.
  • Description du dispositif
    Anterior Cervical Fusion Pack, part number AMS2502(A || Anterior Cervical Fusion Pack, part number AMS2502(C
  • Manufacturer
    Windstone Medical Packaging, Inc.