Astura Medical, LLC is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Astura Medical, LLC - FDA 510(k) Cleared Devices
Recent clearances: SIRION Lateral Lumbar Interbody Fusion, DOLOMITE Anterior Cervical Stabilization System, EL CAPITAN Anterior Lumber Interbody System
8
Total
8
Cleared
0
Denied
Astura Medical, LLC has 8 FDA 510(k) cleared medical devices. Based in Carlsbad, US.
Last cleared in 2021. Active since 2018. Primary specialty: Orthopedic.
Browse the FDA 510(k) cleared devices submitted by Astura Medical, LLC Filter by specialty or product code using the sidebar.
FDA 510(k) Regulatory Record - Astura Medical, LLC
8 devices
Cleared
Jan 06, 2021
SIRION Lateral Lumbar Interbody Fusion
Orthopedic
128d
Cleared
Oct 26, 2020
DOLOMITE Anterior Cervical Stabilization System
Orthopedic
91d
Cleared
Apr 21, 2020
EL CAPITAN Anterior Lumber Interbody System
Orthopedic
223d
Cleared
Apr 02, 2020
SIRION Lateral Lumbar Interbody System
Orthopedic
248d
Cleared
Oct 24, 2019
ALTA Anterior Cervical Corpectomy System
Orthopedic
244d
Cleared
May 03, 2019
HALF DOME Posterior Lumbar Interbody System
Orthopedic
200d
Cleared
Oct 18, 2018
OLYMPIC Posterior Spinal Fixation System
Orthopedic
59d
Cleared
Jul 06, 2018
OLYMPIC Posterior Spinal Fixation System
Orthopedic
67d