ClearanceBrief
510(k) K022374 ยท KWP Appliance, Fixation, Spinal Interlaminal

CADENCE SPINAL FIXATION SYSTEM

ApplicantSulzer Spine-Tech, Minneapolis MN, US
DecisionSubstantially Equivalent, Sep 24, 2002
ReceivedJul 22, 2002
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K022374

DateFirm and productCodeLinked 510(k)
Nov 16, 2006Zimmer Spine, Inc.
Zimmer Spine ST360 Distal Thread Reduction Guide Pins, Part number: 07.00684.00. Non-Sterile. Zimmer Spine, Inc., 7375 Bush Lake Road, Minneapolis, MN 55439 U.S.A. The Distal Thread Reduction Gui
Terminated
KWPNone listed

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