ClearanceBrief
510(k) K181947 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Persona Revision Knee System

ApplicantZimmer, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Oct 25, 2018
ReceivedJul 20, 2018
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K181947

DateFirm and productCodeLinked 510(k)
Jun 24, 2026Zimmer, Inc.
Brand Name: Persona Revision Product Name: Persona Revision Trabecular Metal Femoral Distal Augment Model/Catalog Number: 42-5572-066-10 Software Version: N/A Product Description: Persona Revision Tra
Open, Classified
MBHNone listed

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