Camber Spine Technologies - FDA 510(k) Cleared Devices
17
Total
17
Cleared
0
Denied
Camber Spine Technologies has 17 FDA 510(k) cleared orthopedic devices. Based in Newtown Square, US.
Latest FDA clearance: Jul 2024. Active since 2013.
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 MRC Global, LLC, Mcra, LLC and MRC Global.
17 devices
Cleared
Jul 12, 2024
SPIRA® Anterior Lumbar Spacers
Orthopedic
203d
Cleared
Feb 27, 2024
Camber Sacroiliac (SI) Fixation System
Orthopedic
74d
Cleared
Jul 11, 2023
SPIRA® Posterior Lumbar Spacers
Orthopedic
99d
Cleared
Mar 30, 2023
ENZA-O Titanium Lateral Anterior Lumbar Interbody Fusion (ALIF)
Orthopedic
328d
Cleared
Mar 22, 2023
SPIRA®-C Integrated Fixation System
Orthopedic
90d
Cleared
Apr 29, 2022
Camber Spine Navigation System
Orthopedic
114d
Cleared
Apr 24, 2020
SPIRA-C Integrated Fixation System
Orthopedic
163d
Cleared
Sep 23, 2019
SPIRA Open Matrix ALIF and LLIF
Orthopedic
208d
Cleared
Apr 18, 2018
ENZA-A Titanium ALIF
Orthopedic
167d
Cleared
Feb 02, 2018
Camber Spine Technologies SPIRA - V™ Open Matrix Corpectomy Cage
Orthopedic
50d
Cleared
Nov 07, 2017
SPIRA-C Open Matrix Cervical Interbody
Orthopedic
85d
Cleared
Sep 15, 2017
Ti-Diagon Oblique TLIF
Orthopedic
70d