ClearanceBrief
510(k) K071417 ยท MBH Prosthesis, Knee, Patello/Femorotibial, Semi-Constrained, Uncemented, Porous, Coated, Polymer/Metal/Polymer

DEPUY LPS DIAPHYSEAL AND METAPHYSEAL SLEEVES

ApplicantDePuy Orthopaedics, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Aug 2, 2007
ReceivedMay 21, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K071417

DateFirm and productCodeLinked 510(k)
Feb 15, 2013DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bo
Terminated
MBHNone listed
Feb 15, 2013DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bo
Terminated
MBHNone listed
Feb 15, 2013DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bo
Terminated
MBHNone listed
Feb 15, 2013DePuy Orthopaedics, Inc.
LPS Diaphyseal Sleeves Product Usage: The LPS Diaphyseal Sleeves are used with the LPS System which is an end-stage revision knee product that allows surgeons to reconstruct severe soft tissue and bo
Terminated
MBHNone listed

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