ClearanceBrief
510(k) K053567 ยท HRX Arthroscope

ATHROCARE TOPAZ ARTHROWANDS

ApplicantArthrocare Corp., Sunnyvale CA, US
DecisionSubstantially Equivalent, Mar 6, 2006
ReceivedDec 22, 2005
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K053567

DateFirm and productCodeLinked 510(k)
Sep 16, 2008ArthroCare Corporation
ArthroCare brand Topaz XL ArthroWand with Integrated Cable Wand, Catalog Number: AC4045-01; Product is manufactured and distributed by ArthroCare Corporation, Sunnyvale, CA - Sterile Surgical Device.
Terminated
HRXNone listed

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