ClearanceBrief
510(k) K223529 ยท NKB Thoracolumbosacral Pedicle Screw System

PressON Spinal Fixation System

ApplicantNexus Spine, LLC, Salt Lake City UT, US
DecisionSubstantially Equivalent, May 2, 2023
ReceivedNov 23, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223529

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.