ClearanceBrief
510(k) K081790 ยท MNI Orthosis, Spinal Pedicle Fixation

MODIFICATION TO SINGLE PLANAR MULTI AXIS (SPMA) PEDICLE SCREW SYSTEM

ApplicantTrinity Orthopedics, LLC, San Diego CA, US
DecisionSubstantially Equivalent, Jul 24, 2008
ReceivedJun 25, 2008
TypeSpecial
FDA recordOpen on fda.gov

Recalls that name K081790

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.