ClearanceBrief
510(k) K203222 ยท NKB Thoracolumbosacral Pedicle Screw System

PERLA TL Posterior Osteosynthesis System

ApplicantSpineart, Plan Les Ouates, CH
DecisionSubstantially Equivalent, Dec 17, 2020
ReceivedNov 2, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203222

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.