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.

Apollo Endosurgery

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

Total Devices2
Categories1
Latest FDA decision2019-08-29
TypeNumberDevice NameCodeDateActions
510(k) K191439 OverStitch 2-0 Polypropylene SutureOCW2019-08-29 View
510(k) K181141 OverStitch Endoscopic Suturing System and AccessoriesOCW2018-06-27 View