ClearanceBrief
510(k) K110763 ยท HWC Screw, Fixation, Bone

LATARJET CORTICAL SCREW SET

ApplicantT.A.G. Medical Products Corporation, Ltd., Somerset MA, US
DecisionSubstantially Equivalent, Apr 11, 2011
ReceivedMar 18, 2011
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K110763

DateFirm and productCodeLinked 510(k)
May 12, 2017DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek LATARJET EXPERIENCE-Combo Screw Driver Product Code: 288211 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the antero
Terminated
HWCNone listed
May 12, 2017DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek LATARJET EXPERIENCE Coracoid Drill Product Code: 288201 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferi
Terminated
HWCNone listed
May 12, 2017DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek LATARJET EXPERIENCE Coracoid Top Hat Drill Product Code: 288202 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the ante
Terminated
HWCNone listed
May 12, 2017DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek LATARJET EXPERIENCE Top Hat Tap Product Code: 288203 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroinferior
Terminated
HWCNone listed
May 12, 2017DePuy Mitek, Inc., a Johnson & Johnson Co.
DePuy Mitek LATARJET EXPERIENCE Extraction Driver Product Code: 288216 Product Usage: The Latarjet Cortical Screw set is intended to treat recurrent shoulder instability by supporting the anteroin
Terminated
HWCNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.