ClearanceBrief
510(k) K002281 ยท JWH Prosthesis, Knee, Patellofemorotibial, Semi-Constrained, Cemented, Polymer/Metal/Polymer

STELKAST PROVEN KNEE SYSTEM

ApplicantStelkast Company, Pittsburgh PA, US
DecisionSubstantially Equivalent, Aug 17, 2000
ReceivedJul 24, 2000
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K002281

DateFirm and productCodeLinked 510(k)
Feb 3, 2005Stelkast Co
Proven Porous CR Femur. Implantable orthopedic device
Terminated
JWHNone listed

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