Devices

Device Recall Triathlon TS Femoral Trial

  • Model / Serial
    Lot codes:N4XMPD,WFDC,
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 4 Right || Non-Sterile || Catalog Number: 5512-T-402 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
  • 1 Event

Manufacturer

Stryker Howmedica Osteonics Corp.
  • Manufacturer Address
    Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2002
  • Manufacturer Parent Company (2017)
    Stryker
  • Source
    USFDA

15 devices with a similar name

Learn more about the data here

Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot codeL WFLD
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 1 Left || Non-Sterile || Catalog number 5512-T-101 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot Code WFLI
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 1 Right || Non-Sterile || Catalog number: 5512-T-102 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot code WFLV
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 2 Left || Non-Sterile || Catalog Number 5512-T-201 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Lot Code TYHMPD, WFCP.
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 2 Right || Non-Sterile || Catalog Number: 5512-T-202 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
Device Recall Triathlon TS Femoral Trial
  • Model / Serial
    Code Numbers N4TMPD, PDAMPD, WEWC
  • Product Classification
    Orthopedic Devices
  • Device Class
    1
  • Implanted device?
    No
  • Distribution
    Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
  • Product Description
    Triathlon TS Femoral Trial; || Size 3 Left || Non-Sterile || Catalog Number: 5512-T-301 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Orthopedic Manual Surgical Instrument indicated for use in revision Total Knee Arthroplasty.
  • Manufacturer
    Stryker Howmedica Osteonics Corp.
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