ClearanceBrief
510(k) K232889 ยท JEY Plate, Bone

METICULY Patient-specific titanium maxillofacial mesh implant

ApplicantMeticuly Co., Ltd., Bangkok, TH
DecisionSubstantially Equivalent, Apr 30, 2024
ReceivedSep 18, 2023
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K232889

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.