ClearanceBrief
510(k) K162995 · NKB Thoracolumbosacral Pedicle Screw System

Ibis® Pedicle Screw System

ApplicantOrtho Development Corporation, Draper UT, US
DecisionSubstantially Equivalent, Mar 30, 2017
ReceivedOct 27, 2016
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K162995

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.