ClearanceBrief
510(k) K031595 ยท KWP Appliance, Fixation, Spinal Interlaminal

U & I AMERICA SPINAL HOOK SYSTEM

ApplicantU&I Corp., America, Murray UT, US
DecisionSubstantially Equivalent, Jun 24, 2003
ReceivedMay 21, 2003
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K031595

DateFirm and productCodeLinked 510(k)
Sep 8, 2004U&I America
Optima Spinal System and Spinal Hook System, set screw component.
Terminated
MNINone listed
Feb 27, 2004U&I America
2.5mm Hex Driver
Terminated
MNINone listed
Feb 27, 2004U&I America
4mm Hex Driver
Terminated
MNINone listed

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