ClearanceBrief
510(k) K173518 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

Spectrum Spine Expandable Cages (SSEC)

ApplicantSpectrum Spine, LLC, Atlanta GA, US
DecisionSubstantially Equivalent, Mar 7, 2019
ReceivedNov 14, 2017
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K173518

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.