co_sos
1 records
fda
2 records
FDA Recall: AlloSource, Inc. — Class II
20140514
The donor was hemodiluted. | Product: AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthopedic applications as
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FDA Device Recall: AlloFuse DBM Putty 5cc, Catalog No. 90038005 AlloFuse is indicated for orthop
2014-05-14
Class II — The donor was hemodiluted.
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irs_exempt
2 records
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