ClearanceBrief
510(k) K925160 ยท HRX Arthroscope

ARTHRO FMS 4

ApplicantOrthoconcept, Inc., New York City NY, US
DecisionSubstantially Equivalent, Feb 17, 1994
ReceivedOct 13, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K925160

No recall in the FDA data names this 510(k).

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