ClearanceBrief
510(k) K192680 · NKB Thoracolumbosacral Pedicle Screw System

Percusys® Plus Pedicle Screw System

ApplicantJoimax GmbH, Karlsruhe, DE
DecisionSubstantially Equivalent, Dec 18, 2019
ReceivedSep 26, 2019
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K192680

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.