ClearanceBrief
510(k) K051223 ยท LZO Prosthesis, Hip, Semi-Constrained, Metal/Ceramic/Polymer, Cemented Or Non-Porous, Uncemented

HIPSTAR FEMORAL STEM

ApplicantStryker Orthopaedics, Mahwah NJ, US
DecisionSubstantially Equivalent, May 10, 2006
ReceivedMay 12, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K051223

DateFirm and productCodeLinked 510(k)
Oct 31, 2008Stryker Howmedica Osteonics Corp.
Hipstar V40 Femoral Stem Howemedica: Benoist Girard et Cie; 203 bd de la Grande Selle B.P.8; 14201 Herouville Saint Clair. Used in total and hemi hip arthroplasty for: noninflammatory degenerative j
Terminated
LZONone listed

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