ClearanceBrief
510(k) K223413 · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar

Pisces™-SA STANDALONE ALIF Interbody System

ApplicantOsseus Fusion Systems, Dallas TX, US
DecisionSubstantially Equivalent, Feb 10, 2023
ReceivedNov 9, 2022
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K223413

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.