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Créditos
Devices
Device Recall Triathlon TS Femoral Trial
Modelo / Serial
Lot Code WFJY
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Descripción del producto
Triathlon TS Femoral Trial; || Size 8 Left || Non-Sterile || Catalog Number: 5512-T-801 || 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
Retiro De Equipo (Recall) de Device Recall Triathlon TS Femoral Trial
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Fabricante
Stryker Howmedica Osteonics Corp.
Dirección del fabricante
Stryker Howmedica Osteonics Corp., 325 Corporate Dr, Mahwah NJ 07430-2002
Empresa matriz del fabricante (2017)
Stryker
Source
USFDA
15 dispositivos con un nombre similar
Más información acerca de la data
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Device Recall Triathlon TS Femoral Trial
Modelo / Serial
Lot codeL WFLD
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Descripción del producto
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
Modelo / Serial
Lot Code WFLI
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Descripción del producto
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
Modelo / Serial
Lot code WFLV
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Descripción del producto
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
Modelo / Serial
Lot Code TYHMPD, WFCP.
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Descripción del producto
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
Modelo / Serial
Code Numbers N4TMPD, PDAMPD, WEWC
Clasificación del producto
Orthopedic Devices
Clase de dispositivo
1
¿Implante?
No
Distribución
Nationwide Distribution --- including states of CT, NJ, PA, VA, NC, GA, FL, AL, MI, MN, IL, TX and AZ.
Descripción del producto
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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