ClearanceBrief
510(k) K243602 ยท HRX Arthroscope

Arthrex Spine Endoscope

ApplicantArthrex, Inc., Naples FL, US
DecisionSubstantially Equivalent, May 16, 2025
ReceivedNov 21, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K243602

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.