ClearanceBrief
510(k) K081906 ยท KWP Appliance, Fixation, Spinal Interlaminal

PROTEX CT CERVICOTHORACIC SPINAL SYSTEM

ApplicantGlobus Medical, Inc., Audubon PA, US
DecisionSubstantially Equivalent, Nov 14, 2008
ReceivedJul 3, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081906

No recall in the FDA data names this 510(k).

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