ClearanceBrief
510(k) K033810 ยท HRY Prosthesis, Knee, Femorotibial, Semi-Constrained, Cemented, Metal/Polymer

NATURAL-KNEE II UNICOMPARTMENTAL KNEE SYSTEM

ApplicantCenterpulse Orthopedics, Inc., Austin TX, US
DecisionSubstantially Equivalent, Mar 5, 2004
ReceivedDec 8, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K033810

DateFirm and productCodeLinked 510(k)
Mar 20, 2014Zimmer, Inc.
Natural-Knee II Unicompartmental Knee System: UNI ALL-POLY TIB SZ 1-7mm UNI ALL-POLY TIB SZ 1-9mm
Terminated
HRYNone listed

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