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U.S. Department of Health and Human Services

Medical Device Recalls
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1 to 7 of 7 Results
510(K) Number: K062170
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DePuy Mitek BIOKNOTLESS Plus w/ Panacryl-Indicated for use in soft tissue to bone fixation in associ... 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek BIOKNOTLESS Rapid W/ OC-Indicated for use in soft tissue to bone fixation in association... 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek BIOKNOTLESS Plus w/ Ethibond-Iindicated for use in soft tissue to bone fixation in assoc... 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek BIOKNOTLESS Rapid w/ Pan-Indicated for use in soft tissue to bone fixation in associatio... 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek BIOKNOTLESS Plus w/ OC-Indicated for use in soft tissue to bone fixation in association ... 2 06/02/2023 DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek Lupine Loop Plus w/ Orthocord DS Catalog #210709 The LUPINE BR Anchor System is... 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek Lupine Loop Plus w/ Orthocord Catalog #210708 The LUPINE BR Anchor System is i... 2 11/30/2011 DePuy Mitek, Inc., a Johnson & Johnson Co.
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