Neurostructures, Inc. is one of 5511 FDA 510(k) medical device manufacturers from United States in the dataset, ranked by real submission volume.
Neurostructures, Inc. - FDA 510(k) Cleared Devices
Recent clearances: Cavetto-SA Cervical Cage System, Cavetto [MAX] Cervical Cage System, Transept Cervical Plate System
15
Total
15
Cleared
0
Denied
Neurostructures, Inc. has 15 FDA 510(k) cleared orthopedic devices. Based in Colorado Springs, US.
Historical record: 15 cleared submissions from 2014 to 2020.
Browse the complete list of FDA 510(k) cleared orthopedic devices from this manufacturer. Filter by specialty or product code using the sidebar.
Regulatory submissions have been managed by Empirical Testing Corp and Empirical Consulting.
FDA 510(k) Regulatory Record - Neurostructures, Inc.
15 devices
Cleared
Sep 24, 2020
Cavetto-SA Cervical Cage System
Orthopedic
247d
Cleared
Sep 03, 2020
Cavetto [MAX] Cervical Cage System
Orthopedic
66d
Cleared
Jul 24, 2020
Transept Cervical Plate System
Orthopedic
108d
Cleared
Nov 25, 2019
Cortina™ [MAX] Lumbar Cage System
Orthopedic
98d
Cleared
Nov 09, 2018
Arco™-SA Lumbar Cage System
Orthopedic
87d
Cleared
Nov 08, 2018
Neurostructures Cavetto® [MAX] Cervical Cage System
Orthopedic
143d
Cleared
Mar 29, 2018
Arco™-SA Lumbar Cage System
Orthopedic
181d
Cleared
Mar 22, 2018
Cortina [MAX] Lumbar Cage System
Orthopedic
34d
Cleared
Feb 26, 2018
Neurostructures Cavetto® Cervical Cage System
Orthopedic
209d
Cleared
Feb 23, 2018
Cavetto-SA Cervical Cage System
Orthopedic
147d
Cleared
Oct 25, 2017
Cortina™ Lumbar Cage System
Orthopedic
121d
Cleared
Jun 08, 2017
Trifore(tm) Cervical Plating System
Orthopedic
55d
Cleared
Jul 15, 2016
Belvedere™ Lateral Plating System
Orthopedic
263d
Cleared
Feb 25, 2015
Palladian Lumbar Pedicle Screw System
Orthopedic
107d
Cleared
Nov 18, 2014
TRANSOM ANTERIOR CERVICAL PLATE
Orthopedic
112d