ClearanceBrief
510(k) K980358 ยท KWP Appliance, Fixation, Spinal Interlaminal

SYNTHES SPINE POSTERIOR CERVICAL/THORACIC HOOK/ROD SYSTEM

ApplicantSynthes (Usa), Paoli PA, US
DecisionSubstantially Equivalent, Apr 16, 1998
ReceivedJan 29, 1998
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K980358

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.