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.

Binder Biomedical, Inc.

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

Total Devices2
Categories0
Latest FDA decision
TypeNumberDevice NameCodeDateActions
510(k) K130641 LOGIC STAND-ALONE INTERVERTEBRAL BODY FUSION DEVICEOVD2013-09-13 View
510(k) K093015 BINDER INTERVERTEBRAL BODY FUSION DEVICEMAX2010-02-25 View
↑