ClearanceBrief
510(k) K203282 ยท JEY Plate, Bone

TECHFIT Patient-Specific Maxillofacial System

ApplicantIndustrias Medicas Sampedro S.A.S, La Estrella, CO
DecisionSubstantially Equivalent, May 19, 2021
ReceivedNov 6, 2020
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K203282

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.