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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: K024366
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Medtronic SPYDER Anastomotic Device. Sterilized using irradiation. Do not Reuse. Nonpyrogenic. T... 2 04/13/2006 FEI # 3003368396
Medtronic Cardiac Surgery Technologies
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