ClearanceBrief
510(k) K150394 ยท PLF Bone Wedge

Tyber Medical Wedge System

ApplicantTyber Medical, LLC, Morristown NJ, US
DecisionSubstantially Equivalent, Jul 28, 2015
ReceivedFeb 18, 2015
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K150394

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.