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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K062789
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Product Description
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Recall
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FDA Recall
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1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 24 mm - Sterile, Rapid Resorbable Fixation Syst... 2 06/07/2016 Synthes (USA) Products LLC
1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 35 mm - Sterile, Rapid Resorbable Fixation Syst... 2 06/07/2016 Synthes (USA) Products LLC
1.5 mm Rapid Resorb Orbt1 F1 P1 w/Bending Template / 30 mm - Sterile, Rapid Resorbable Fixation Syst... 2 06/07/2016 Synthes (USA) Products LLC
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