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U.S. Department of Health and Human Services

Medical Device Recalls
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1 result found
510(K) Number: K040168
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FDA Recall
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Spinal Implant, Catalog number: 1000-3000 through 1000-3015 (9 catalog numbers) 2 02/04/2005 FEI # 1000160576
Interpore Cross International Inc
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