ClearanceBrief
510(k) K120174 ยท PHX Shoulder Prosthesis, Reverse Configuration

DEPUT DELTA XTEND REVERSE SHOULDER

ApplicantDepuy France, Warsaw IN, US
DecisionSubstantially Equivalent, Jun 11, 2012
ReceivedJan 20, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K120174

DateFirm and productCodeLinked 510(k)
Aug 31, 2017DePuy Orthopaedics, Inc.
DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants are intended for use in total shoulder or hemi-shoulder replacement procedures in patients with non-functional ro
Terminated
HSDNone listed
Aug 31, 2017DePuy Orthopaedics, Inc.
DELTA XTEND" Reverse Shoulder System Modular Centered and Eccentric Epiphysis Implants intended for use in total shoulder or hemi-shoulder replacement procedures in patients with non-functional rotato
Terminated
KWSNone listed

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