ClearanceBrief
510(k) K922292 ยท MJW Prosthesis, Subtalar, Plug, Polymer

LUNDEEN SUBTALAR PEG IMPLANT

ApplicantSgarlato Laboratories, Inc., San Jose CA, US
DecisionSubstantially Equivalent, Oct 23, 1992
ReceivedMay 15, 1992
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K922292

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.