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Devices
Device Recall Stem Trial, Triathlon Revision Instruments
Model / Serial
All lot codes
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Canada, Sweden, Germany, Spain, Portugal, United Kingdom.
Product Description
Stem Trial, Triathlon Revision Instruments; Non-Sterile; 100 mm length || Catalog numbers: || 5565-T-009, 5565-T-010, 5565-T-011, 5565-T-012, 5565-T-013, 5565-T-014 || 5565-T-015, 5565-T-016, 5565-T-017, 5565-T-018, 5565-T-019, 5565-T-020 || 5565-T-021, 5565-T-022, 5565-T-023, 5565-T-024, 5565-T-025 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Used in Revision TKA.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
Recall of Device Recall Stem Trial, Triathlon Revision Instruments
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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
One device with a similar name
Learn more about the data
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Device Recall Stem Trial, Triathlon Revision Instruments
Model / Serial
All Lot Codes
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
Worldwide Distribution --- including USA and countries of Australia, Canada, Sweden, Germany, Spain, Portugal, United Kingdom.
Product Description
Stem Trial, Triathlon Revision Instruments; Non-Sterile; 150 mm length || Catalog Numbers: || 5566-T-009, 5566-T-010, 5566-T-011, 5566-T-012, 5566-T-013, 5566-T-014 || 5566-T-015, 5566-T-016, 5566-T-017, 5566-T-018, 5566-T-019, 5566-T-020 || 5566-T-021, 5566-T-022, 5566-T-023, 5566-T-024, 5566-T-025 || Howmedica Osteonics Corp. || 325 Corporate Drive || Mahwah, NJ 07430 || Used in Revision TKA.
Manufacturer
Stryker Howmedica Osteonics Corp.
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