ClearanceBrief
510(k) K951267 ยท HRX Arthroscope

STRYKER UNIVERSAL ACL INSTRUMENTATION SYSTEM

ApplicantStryker Endoscopy, Santa Clara CA, US
DecisionSubstantially Equivalent, Sep 1, 1995
ReceivedMar 21, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K951267

DateFirm and productCodeLinked 510(k)
Apr 2, 2008Stryker Endoscopy
Stryker ACL Workstation slider, Model Number: 234-010-503, Stryker, San Jose, CA 95138
Terminated
HRXNone listed

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