ClearanceBrief
510(k) K970200 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

RELIANCE PF FEMORAL STEMS

ApplicantHowmedica Corp., Rutherford NJ, US
DecisionSubstantially Equivalent, Apr 9, 1997
ReceivedJan 21, 1997
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K970200

DateFirm and productCodeLinked 510(k)
Nov 1, 2005Stryker Howmedica Osteonics Corp.
Reliance PF Femoral Stem
Terminated
MAYNone listed

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