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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 10 of 27 Results
Date Classified to: 04/20/2014 510(K) Number: K093235
 
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Ringloc + Acetabular Shell limited hole finned 46 mm Size 22 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole, 76 mm Size 28, porous coat, for uncemented use, sterile, RE... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 50 mm Size 23 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 52 mm Size 23 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 54 mm Size 24 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 56 mm Size 24 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 58 mm Size 25 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 60 mm Size 25 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 62 mm Size 26 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
Ringloc + Acetabular Shell limited hole finned 64 mm Size 26 porous coat, for uncemented use, steril... 2 Jun-08-2011 Biomet, Inc.
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