ClearanceBrief
510(k) K242480 ยท HAW Neurological Stereotaxic Instrument

FLASH EVD System (10-0002)

Applicant7D Surgical ULC, Toronto, CA
DecisionSubstantially Equivalent, Dec 27, 2024
ReceivedAug 21, 2024
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K242480

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.