ClearanceBrief
510(k) K062029 ยท KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

ANATOMICAL SHOULDER FRACTURE SYSTEM

ApplicantZimmer GmbH, Warsaw IN, US
DecisionSubstantially Equivalent, Oct 31, 2006
ReceivedJul 18, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K062029

DateFirm and productCodeLinked 510(k)
Nov 6, 2012Zimmer, Inc.
Anatomical Shoulder" Fracture Humeral stem
Terminated
KWSNone listed
Nov 6, 2012Zimmer, Inc.
Anatomical Shoulder" Revision Humeral stem,7,9,12,14 and Anatomical Shoulder Fracture Humeral stem
Terminated
KWSNone listed
Nov 6, 2012Zimmer, Inc.
Anatomical Shoulder" Fracture Humeral Head
Terminated
KWSNone listed

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