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U.S. Department of Health and Human Services

Medical Device Recalls
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Z-0907-2015 - Ti-Bond Marketing Literature/Labeling, Catalog No. LT10000, MP-14000 This device is intended to be used with autogenous bone graft. Patients must have undergone a regimen of at least six (6) months n... 2 01/05/2015 FEI # 3004893332
Spinal Elements, Inc
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