ClearanceBrief
510(k) K900930 ยท HQX Implant, Orbital, Extra-Ocular

SPIVEY-ALLEN ORBITAL FLOOR IMPLANT

ApplicantOculo Plastik, Inc., Montreal, Quebec Canada, CA
DecisionSubstantially Equivalent, May 15, 1990
ReceivedFeb 27, 1990
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K900930

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.