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U.S. Department of Health and Human Services

Medical Device Recalls
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510(K) Number: K120559
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FDA Recall
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Miethke Shunt System accessories Product Usage: - The Miethke Shunt System is intended to shut ... 2 01/26/2015 FEI # 2916714
Aesculap, Inc.
Aesculap proSA Adjustment Disc Size Large (L) The Miethke proSA Adjustment shunt system is intend... 2 02/19/2014 FEI # 2916714
Aesculap, Inc.
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