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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: K080685
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Product Description
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FDA Recall
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HipLOC Hip Fracture Fixation System- Hiploc System 130¿ Plate 38 mm Barrel 4 Hole Plate Item Number... 2 09/27/2018 FEI # 3002806535
Biomet UK Ltd.
HipLOC Hip Fracture Fixation System-Hiploc System 140¿ Plate 38 mm Barrel 4 Hole Plate Item Number:... 2 09/27/2018 FEI # 3002806535
Biomet UK Ltd.
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 4 Hole Plate Item Number:... 2 09/27/2018 FEI # 3002806535
Biomet UK Ltd.
HipLOC Hip Fracture Fixation System-Hiploc System 135¿ Plate 38 mm Barrel 3 Hole Plate Item Numbe... 2 09/27/2018 FEI # 3002806535
Biomet UK Ltd.
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