ClearanceBrief
510(k) K123623 ยท NKB Thoracolumbosacral Pedicle Screw System

ILLICO MIS POSTERIOR FIXATION SYSTEM

ApplicantAlphatec Spine, Inc., Carlsnad CA, US
DecisionSubstantially Equivalent, Feb 14, 2013
ReceivedNov 23, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123623

DateFirm and productCodeLinked 510(k)
Aug 27, 2013Alphatec Spine, Inc.
Illico Ti Cannulated Polyaxial Screw 7.5mm X 40mm. The Illico MIS Posterior Fixation System is intended to facilitate the surgical correction of noncervical spinal deformities by providing temporary i
Terminated
NKBNone listed

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