Medical Device Manufacturer · US , Chesterland , OH

Nexxt Spine, LLC - FDA 510(k) Cleared Devices

22 submissions · 22 cleared · Since 2009
22
Total
22
Cleared
0
Denied

Nexxt Spine, LLC has 22 FDA 510(k) cleared orthopedic devices. Based in Chesterland, US.

Last cleared in 2023. Active since 2009.

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 Backroads Consulting and Backroads Consulting, Inc..

FDA 510(k) Regulatory Record - Nexxt Spine, LLC
22 devices
1-12 of 22
Cleared Jul 20, 2023
INERTIA® CONNEXX™ Modular Pedicle Screw System
K231799 · NKB
Orthopedic · 30d
Cleared Jul 28, 2022
INERTIA CONNEXX Modular Pedicle Screw System
K221905 · NKB
Orthopedic · 28d
Cleared Mar 31, 2022
NEXXT SPINE NAVIGATION System
K220291 · OLO
Orthopedic · 58d
Cleared Dec 15, 2020
NEXXT MATRIXX Stand Alone ALIF System
K202230 · OVD
Orthopedic · 130d
Cleared Sep 17, 2020
STRUXXURE®-L and STRUXXURE®-A Plate System
K202192 · KWQ
Orthopedic · 43d
Cleared May 21, 2020
NEXXT MATRIXX System
K200969 · MAX
Orthopedic · 38d
Cleared Mar 23, 2020
NEXXT MATRIXX Stand Alone Cervical-Turn Lock (-TL) System
K200543 · OVE
Orthopedic · 20d
Cleared Feb 24, 2020
NEXXT MATRIXX System
K193412 · PLR
Orthopedic · 77d
Cleared Jan 21, 2020
Nexxt Matrixx System
K193370 · MAX
Orthopedic · 47d
Cleared Jan 09, 2020
TrellOss™-L MPF
K192687 · MAX
Orthopedic · 105d
Cleared Jul 10, 2019
Nexxt Matrixx System
K191408 · MAX
Orthopedic · 43d
Cleared May 31, 2019
NEXXT MATRIXX Stand Alone Cervical System
K190546 · OVE
Orthopedic · 87d
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