Devices

Device Recall TRI PRESSFIT STEM

Model / Serial
5565-S-015 TRI PRESS-FIT STEM 15MM X 100MM M3M07B, 5565-S-016 TRI PRESS-FIT STEM 16MM X 100MM M3M01B, 5565-S-016 TRI PRESS-FIT STEM 16MM X 100MM M3M01E, 5565-S-017 TRI PRESS-FIT STEM 17MM X 100MM M3M03A, 5566-S-012 TRI PRESS-FIT STEM 12X150MM M3L11F, 5566-S-013 TRI PRESS-FIT STEM 13X150MM M3L12B, and 5566-S-018 TRI PRESS-FIT STEM 18X150MM M3L17D
Product Classification
Orthopedic Devices
Device Class
2
Implanted device?
Yes
Distribution
Nationwide. OUS: Australia, Canada, Japan, Argentina, Brazil, Germany, Spain, Columbia, Guatemala and Sweden.
Product Description
Triathlon-Press-Fit Stem || These devices are modular components of a total knee system. These modular stems are intended for use with femoral and tibial components in primary or revision total knee arthroplasty.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
- Recall of Device Recall TRI PRESSFIT STEM

Manufacturer

Stryker Howmedica Osteonics Corp.

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

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Medical devices help to diagnose, prevent and treat many injuries and diseases. We are not suggesting or implying that any companies or other entities included in the International Medical Devices Database engaged in unlawful conduct or otherwise acted improperly. The same device may have different names in different countries. This database is not intended to provide medical advice and patients should check with their doctors to determine if it contains relevant information and if such information has medical implications for them.

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