ClearanceBrief
510(k) K201614 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

TxTiHA IBF System, AxTiHA Stand-Alone ALIF System

ApplicantInnovasis, Inc., Salt Lake City UT, US
DecisionSubstantially Equivalent, Jul 15, 2020
ReceivedJun 15, 2020
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K201614

DateFirm and productCodeLinked 510(k)
Sep 17, 2024Innovasis, Inc
TxHA PEEK IBF/TxTiHA IBF System REF BTA-151 i. TxHA The Innovasis TxHA PEEK IBF System is an intervertebral body fusion device intended to stabilize a spinal segment to promote fusion using bone gr
Open, Classified
MAXNone listed

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.