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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 4 of 4 Results
510(K) Number: K984209
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Product Description
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Recall
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FDA Recall
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TI Cannulated Screw 20MM thrd 6.5MM (d) X 85MM (L); Trauma Fixation Systems, Rx Only; Biomet, 100 ... 3 09/22/2009 EBI, L.P.
TI Cannulated Screw 32MM thrd 7.3MM (d) X 120MM (L); Trauma Fixation Systems, Rx Only; Biomet, 100... 3 09/22/2009 EBI, L.P.
TI Cannulated Screw 32MM thrd 7.3MM (d) X 100MM (L); Trauma Fixation Systems, Rx Only; Biomet, 100... 3 09/22/2009 EBI, L.P.
TI Cannulated Screw 32MM thrd 7.3MM (d) X 95MM (L); Trauma Fixation Systems, Rx Only; Biomet, 100 ... 3 09/22/2009 EBI, L.P.
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