ClearanceBrief
510(k) K200235 ยท MQP Spinal Vertebral Body Replacement Device

KONG-TL VBR System, KONG-C VBR System

ApplicantIcotec AG, Altstaetten, CH
DecisionSubstantially Equivalent, May 29, 2020
ReceivedJan 30, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K200235

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.