ClearanceBrief
510(k) K850886 ยท KIT Media And Components, Synthetic Cell And Tissue Culture

COMPRESSION HIP SCREW SYSTEM

ApplicantPfizer, Inc., Ny NY, US
DecisionSubstantially Equivalent, Apr 19, 1985
ReceivedMar 4, 1985
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K850886

DateFirm and productCodeLinked 510(k)
Sep 16, 2008Stryker Howmedica Osteonics Corp.
Short Barrel Sideplate, Omega + 140 degrees, 4 slots; The Omega Plus Compression Screw system consists of a series of lag screws, proximal hip side plates, supracondylar side plates, and compression s
Terminated
KTTNone listed

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