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.

Nanovis, LLC

FDA 510(k) & PMA Approved Devices — 7 products

Total Devices7
Categories3
Latest FDA decision2024-09-05
TypeNumberDevice NameCodeDateActions
510(k) K241605 Adaptix™ PEEK Interbody System with Nanotechnology; Capstone Control™ PEEK Spinal System with NanotechnologyMAX2024-09-05 View
510(k) K230936 Anatomic PEEK™ Cervical Fusion System with NanotechnologyODP2023-06-02 View
510(k) K203452 Nano FortiFix® SystemNKB2020-12-22 View
510(k) K191822 Nano FortiCore, FortiCoreODP2019-10-11 View
510(k) K171312 FortiCore®MAX2018-01-22 View
510(k) K161485 Nanovis Intervertebral Body Fusion System and Forticore(R)MAX2016-09-06 View
510(k) K160874 Nanovis Intervertebral Body Fusion System and FortiCore®MAX2016-06-28 View
↑