fda
2 records
FDA Recall: Synvasive Technology Inc — Class II
20130424
Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade. | Product: The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For use wit...
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FDA Device Recall: The Oxford Partial Knee; Oxford Knee Resection Procedure 3 Pack CEMENTED For us
2013-04-24
Class II — Biomet part # 506076, lot 928182 was received from Synvasive Technology containing the incorrect blade.
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