Devices

Device Recall Stryker Orthopaedics Triathlon Tritanium Patella Inserter

Model / Serial
Catalog No. 6541-3-530. Lot Codes: CTD2778 and CTD2779.
Product Classification
Orthopedic Devices
Device Class
1
Implanted device?
No
Distribution
US Nationwide Distribution - in the states of Arizona, Florida, Kentucky, Louisiana and New Jersey.
Product Description
Stryker Orthopaedics Triathlon Tritanium Patella Inserter, . NON-STERILE || Product Usage: || The Triathlon Tritanium Patella Inserter is part of the Tritanium Knee System Instrument Set. It is used to implant the Tritanium Patella after the patellar bone has been prepared using the existing Triathlon Patella Resection Guide, Metal Backed Patella Drill and Patella Peg Drill Templates as per the Triathlon Tritanium Surgical Protocol.
Manufacturer
Stryker Howmedica Osteonics Corp.
1 Event
- Recall of Device Recall Stryker Orthopaedics Triathlon Tritanium Patella Inserter

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

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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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