ClearanceBrief
510(k) K070295 ยท MNI Orthosis, Spinal Pedicle Fixation

SINGLE PLANAR MULTI AXIAL (SPMA) PEDICLE SCREW SYSTEM

ApplicantTrinity Orthopedics, LLC, San Diego, CA, US
DecisionSubstantially Equivalent, May 21, 2007
ReceivedJan 31, 2007
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K070295

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.