ClearanceBrief
510(k) K210551 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

Persona Revision Knee System

ApplicantZimmer, Inc., Warsaw IN, US
DecisionSubstantially Equivalent, Mar 18, 2021
ReceivedFeb 25, 2021
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K210551

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.