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U.S. Department of Health and Human Services

Medical Device Recalls

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1 to 3 of 3 Results
510(K) Number: K150600
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Product Description
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Recall
Class
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FDA Recall
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Orthopedics 6.0MM ROD, COCR, SINGLE HEX, 500MM LENGTH-The RESPONSE" 5.5/6.0 Spine System is intended... 2 07/30/2020 OrthoPediatrics Corp
Response 5.5/6.0 Spine System 7.0mm x 40mm Pedicle Screw Product Usage: Posterior non-cervica... 2 02/14/2018 OrthoPediatrics Corp
UniAxial Pedicle Screw & UniAxial Reduction Pedicle Screw The Response 5.5/6.0 Spine System is in... 2 01/08/2016 OrthoPediatrics Corp
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