Medical Device Recalls
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1 to 2 of 2 Results
510(K) Number: K111492 |
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Results per Page |
Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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PATIENT SPECIFIC INSTRUMENTS LPS-FLEX PIN GUIDES (FEMUR AND TIBIA) NONSTERILE ~ MUST BE STERILIZED... | 2 | 05/14/2012 | Materialise USA LLC |
PATIENT SPECIFIC INSTRUMENTS N-K FLEX PIN GUIDES (FEMUR AND TIBIA) NONSTERILE ~ MUST BE STERILIZED... | 2 | 05/14/2012 | Materialise USA LLC |
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