ClearanceBrief
510(k) K202659 ยท HRX Arthroscope

Stryker Arthroscope

ApplicantStryker, San Jose CA, US
DecisionSubstantially Equivalent, Dec 1, 2020
ReceivedSep 14, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K202659

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.