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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 10 of 13 Results
510(K) Number: K051188
 
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Product Description
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FDA Recall
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Grafton DBM Putty Multiple Sizes Grafton is a human bone allograft product containing deminerali... 2 10/18/2012 Osteotech Inc
Grafton DBM Gel Multiple Sizes Grafton is a human bone allograft product containing demineralize... 2 10/18/2012 Osteotech Inc
Grafton DBM Flex Multiple Sizes Grafton is a human bone allograft product containing demineraliz... 2 10/18/2012 Osteotech Inc
Grafton DBM A-Flex Multiple Sizes Grafton is a human bone allograft product containing demineral... 2 10/18/2012 Osteotech Inc
Grafton DBM Crunch Multiple Sizes Grafton is a human bone allograft product containing demineral... 2 10/18/2012 Osteotech Inc
Grafton DBM Matrix PLF Multiple Sizes Grafton is a human bone allograft product containing demin... 2 10/18/2012 Osteotech Inc
Grafton DBM Matrix Strips Multiple Sizes Grafton is a human bone allograft product containing de... 2 10/18/2012 Osteotech Inc
Grafton DBM Orthoblend Small Defect Multiple Sizes Grafton is a human bone allograft product con... 2 10/18/2012 Osteotech Inc
Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product co... 2 10/18/2012 Osteotech Inc
Grafton DBM Orthoblend Large Defect Multiple Sizes Grafton is a human bone allograft product co... 2 10/18/2012 Osteotech Inc
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