ClearanceBrief
510(k) K960025 ยท JDI Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Cemented

PROTEK LOW PROFILE ACETABULAR CUP

ApplicantIntermedics Orthopedics, Austin TX, US
DecisionSubstantially Equivalent, Jun 7, 1996
ReceivedJan 2, 1996
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K960025

DateFirm and productCodeLinked 510(k)
Nov 6, 2012Zimmer, Inc.
Original M.E. Mueller" Low Profile Cup Sterile, Rx
Terminated
JDINone listed

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