Medical Device Manufacturer · US , Colorado Springs , CO

Neurostructures, Inc. - FDA 510(k) Cleared Devices

15 submissions · 15 cleared · Since 2014
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.

FDA 510(k) cleared devices by Neurostructures, Inc.

15 devices
1-12 of 15
Cleared Sep 24, 2020
Cavetto-SA Cervical Cage System
K200115 · OVE
Orthopedic · 247d
Cleared Sep 03, 2020
Cavetto [MAX] Cervical Cage System
K201769 · ODP
Orthopedic · 66d
Cleared Jul 24, 2020
Transept Cervical Plate System
K200927 · KWQ
Orthopedic · 108d
Cleared Nov 25, 2019
Cortina™ [MAX] Lumbar Cage System
K192248 · MAX
Orthopedic · 98d
Cleared Nov 09, 2018
Arco™-SA Lumbar Cage System
K182195 · OVD
Orthopedic · 87d
Cleared Nov 08, 2018
Neurostructures Cavetto® [MAX] Cervical Cage System
K181590 · ODP
Orthopedic · 143d
Cleared Mar 29, 2018
Arco™-SA Lumbar Cage System
K173082 · OVD
Orthopedic · 181d
Cleared Mar 22, 2018
Cortina [MAX] Lumbar Cage System
K180431 · MAX
Orthopedic · 34d
Cleared Feb 26, 2018
Neurostructures Cavetto® Cervical Cage System
K172320 · ODP
Orthopedic · 209d
Cleared Feb 23, 2018
Cavetto-SA Cervical Cage System
K173077 · OVE
Orthopedic · 147d
Cleared Oct 25, 2017
Cortina™ Lumbar Cage System
K171914 · MAX
Orthopedic · 121d
Cleared Jun 08, 2017
Trifore(tm) Cervical Plating System
K171112 · KWQ
Orthopedic · 55d
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