ClearanceBrief
510(k) K800363 ยท KTZ Caliper

PARKE-DAVIS TOTAL KNEE PROSTHESIS

ApplicantWarner-Lambert Co., Mchenry IL, US
DecisionSubstantially Equivalent, Mar 10, 1980
ReceivedFeb 20, 1980
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K800363

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.