ClearanceBrief
510(k) K023644 ยท MNI Orthosis, Spinal Pedicle Fixation

MODIFICATION TO INCOMPASS SPINAL FIXATION SYSTEM

ApplicantSpinal Concepts, Inc., Austin TX, US
DecisionSubstantially Equivalent, Nov 25, 2002
ReceivedOct 30, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K023644

DateFirm and productCodeLinked 510(k)
Sep 1, 2008Abbott Spine
InCompass Spinal Fixation System T-Handle Driver; Part #2151-4 (9.5" shaft) and 2151-5 (13" shaft); Non-sterile, Reusable Instrument; manufactured by Abbott Spine, Austin, TX 78727.
Terminated
MNINone listed

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