ClearanceBrief
510(k) K955632 ยท LZN Cement Obturator

ORTHOPLUG SOFT BONE DESIGN

ApplicantSunmed, Inc., Redding CA, US
DecisionSubstantially Equivalent, Feb 27, 1996
ReceivedDec 11, 1995
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K955632

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.