ClearanceBrief
510(k) K123783 ยท KWP Appliance, Fixation, Spinal Interlaminal

ELLIPSE OCCIPITO-CERICO-THORACIC SPINAL SYSTEM AND CAPITOL IMPLANTS

ApplicantGlobus Medical, Inc., Audubon PA, US
DecisionSubstantially Equivalent, Mar 14, 2013
ReceivedDec 10, 2012
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K123783

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.