ClearanceBrief
510(k) K010811 ยท HRX Arthroscope

PERC-D SPINEWAND

ApplicantArthrocare Corp., Sunnyvale CA, US
DecisionSubstantially Equivalent, May 30, 2001
ReceivedMar 19, 2001
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K010811

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.