Devices

DURACON TOTAL KNEE SYSTEM - HEMIFLAT TIABIAL AUGMENTS

Model / Serial
Model Catalog: 6630-6-275 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-110 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-125 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-130 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-150 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-375 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-370 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-355 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-350 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-325 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-305 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-105 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-270 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-255 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-250 (Lot serial: >10 NUMBERS CONTACT MFG); Model Catalog: 6630-6-230 (Lot serial: >10 NUMBE
Product Description
DURACON TOTAL KNEE SYSTEM - HEMIFLAT TIABIAL AUGMENTS
Manufacturer
STRYKER CANADA LP
1 Event
- Recall of DURACON TOTAL KNEE SYSTEM - HEMIFLAT TIABIAL AUGMENTS

Manufacturer

STRYKER CANADA LP

Manufacturer Address
HAMILTON
Manufacturer Parent Company (2017)
Stryker
Source
HC

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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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