Neos Surgery S.L is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neos Surgery S.L - FDA 510(k) Cleared Devices
Recent clearances: Cranial LOOP, Cranial LOOP L and Cranial LOOP XL Cranial Bone Fixation System, STERN FIX Sternal Stabilization System, Stern Fix Sternal Stabilization System
6
Total
6
Cleared
0
Denied
Neos Surgery S.L has 6 FDA 510(k) cleared medical devices. Based in Alexandria, US.
Latest FDA clearance: Feb 2024. Active since 2010. Primary specialty: Neurology.
Browse the FDA 510(k) cleared devices submitted by Neos Surgery S.L Filter by specialty or product code using the sidebar.
510(k) submissions have been managed by Msquared Associates, Inc. as regulatory consultant.
FDA 510(k) Regulatory Record - Neos Surgery S.L
6 devices
Cleared
Feb 16, 2024
Cranial LOOP, Cranial LOOP L and Cranial LOOP XL Cranial Bone Fixation System
Neurology
29d
Cleared
Oct 19, 2022
STERN FIX Sternal Stabilization System
Orthopedic
120d
Cleared
Jan 19, 2022
Stern Fix Sternal Stabilization System
Orthopedic
238d
Cleared
Jun 12, 2016
Cranial COVER
Neurology
87d
Cleared
Sep 30, 2013
CRANIAL LOOP, CRANIAL LOOP L AND CRANIAL LOOP XL AND CRANIAL BONE FIXATION...
Neurology
90d
Cleared
Oct 25, 2010
CRANIAL LOOP CRANIAL BONE FIXATION SYSTEM
Neurology
175d