ClearanceBrief
510(k) K060735 ยท ITH Equipment, Traction, Powered

DRX9000 TRUE SPINAL DECOMPRESSION SYSTEM

ApplicantAxiom Worldwide, Inc., Tampa FL, US
DecisionSubstantially Equivalent, May 26, 2006
ReceivedMar 20, 2006
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K060735

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.