Aegis Spine is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Aegis Spine - FDA 510(k) Cleared Devices
Recent clearances: ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix Anterior Cervical Plate System, Spinema Lumbar Plate System
1
Total
1
Cleared
0
Denied
Aegis Spine has 1 FDA 510(k) cleared medical devices. Based in Englewood, US.
Last cleared in 2021. Active since 2021. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Aegis Spine Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Empirical Testing Corp as regulatory consultant.
FDA 510(k) Regulatory Record - Aegis Spine
1 devices