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.

AgNovos Healthcare USA, LLC

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

Total Devices2
Categories1
Latest FDA decision2018-07-20
TypeNumberDevice NameCodeDateActions
510(k) K181585 JGH1 Core Deccompression Procedure KitMQV2018-07-20 View
510(k) K181342 JGH1 Bone Graft SubstituteMQV2018-07-19 View