Devices

Lumbar Laminectomy Pack

  • Model / Serial
    Lot numbers/Expiration dates:  64906 11/3/2015 66041 11/6/2015 62111 11/12/2015 65892 12/22/2015 66759 7/29/2016 69271 9/19/2016 68960 9/26/2016 67958 9/28/2016 70334 1/29/2017 74063 5/15/2017 75454 7/8/2017 80958 8/8/2017 78464 9/14/2017 77100 10/25/2017 79659 1/17/2018
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution to California, Florida, Georgia, Illinois, Kansas, Louisiana, Michigan, New Jersey, Nevada, Texas, Virginia, and Wyoming.
  • Product Description
    Lumbar Laminectomy Pack, Kit number AMS2501 || convenience custom kits used for general surgery in hospital operating room
  • Manufacturer
    Windstone Medical Packaging, Inc.
  • 1 Event

Manufacturer

Windstone Medical Packaging, Inc.
  • Manufacturer Address
    Windstone Medical Packaging, Inc., 1602 4th Ave N, Billings MT 59101-1521
  • Manufacturer Parent Company (2017)
    Windstone Medical Packaging Inc.
  • Source
    USFDA

One device with a similar name

Learn more about the data here

Device Recall Lumbar Laminectomy Pack
  • Model / Serial
    Lot number and expiration date  83672, 5/11/2018 84748, 6/3/2018 86722, 8/19/2018 88051, 1/7/2018 89026, 11/21/2018 89027, 12/12/2018 89882, 12/10/2018 94933, 1/29/2019
  • Product Classification
    General and Plastic Surgery Devices
  • Device Class
    2
  • Implanted device?
    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.
  • Product Description
    Lumbar Laminectomy Pack, part number AMS2501 || Lumbar Laminectomy Pack, part number AMS2501(A || Lumbar Laminectomy Pack, part number AMS2501(B
  • Manufacturer
    Windstone Medical Packaging, Inc.