ClearanceBrief
510(k) DEN200010 ยท OQB Intervertebral Body Graft Containment Device

Spineology Interbody Fusion System

ApplicantSpineology, Inc., Saint Paul MN, US
DecisionUnknown, Sep 18, 2020
ReceivedFeb 19, 2020
TypeDirect
FDA recordOpen on fda.gov

Recalls that name DEN200010

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.