Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

Oak Tree Engineering, LLC

FDA 510(k) & PMA Approved Devices — 2 products

Total Devices2
Categories1
Latest FDA decision2022-12-07
TypeNumberDevice NameCodeDateActions
510(k) K220843 OAKTREE Anterior Lumbar Plate and Screw SystemKWQ2022-12-07 View
510(k) K211932 Fixxsure Anterior Lumbar Plate and Screw SystemKWQ2021-07-27 View