ClearanceBrief
510(k) K110927 ยท MAX Intervertebral Fusion Device With Bone Graft, Lumbar

MECTALIF

ApplicantMedacta International, Camarillo CA, US
DecisionSubstantially Equivalent, Jun 13, 2011
ReceivedMar 28, 2011
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K110927

DateFirm and productCodeLinked 510(k)
Nov 18, 2014Medacta Usa
The MectaLIF Oblique Handle, model number 03.22.10.0262, is used to insert the MectaLIF oblique spinal cage implants.
Terminated
MAXNone listed

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