Medical Device Recalls
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1 result found
510(K) Number: K161267 |
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Results per Page |
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Product Description
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Recall
Class |
FDA Recall
Posting Date |
Recalling Firm
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| Response BandLoc 5.5/6.0 Tensioner Instrument The Tensioner Instrument (01-1102-1000) is utilized... | 2 | 06/09/2017 | OrthoPediatrics Corp |
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