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.

Hd Lifesciences, LLC

FDA 510(k) & PMA Approved Devices — 3 products

Total Devices3
Categories3
Latest FDA decision2020-04-28
TypeNumberDevice NameCodeDateActions
510(k) K200541 Hive™ Stand-alone Anterior Lumbar Interbody SystemOVD2020-04-28 View
510(k) K180364 HD LifeSciences Cervical IBFD SystemODP2018-06-27 View
510(k) K170676 HD Lumbar Interbody SystemMAX2017-07-13 View