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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: K171427
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Medtronic Aptus Heli-FX Thoracic EndoAnchor System Heli-FX Guide 42 mm, REF HG-18-90-42, STERILE EO,... 2 09/27/2017 Medtronic Vascular, Inc.
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