ClearanceBrief
510(k) K160820 ยท NKB Thoracolumbosacral Pedicle Screw System

PressON Pro Spinal Fixation System

ApplicantNexus Spine, LLC, Salt Lake City UT, US
DecisionSubstantially Equivalent, Jun 28, 2016
ReceivedMar 24, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K160820

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.