FDA 510(k) Applications Submitted by Cutting Edge Spine, LLC
FDA 510(k) Number |
Submission Date |
Device Name |
Applicant |
K102957 |
10/05/2010 |
CUTTING EDGE SPINE INTERBODY FUSION DEVICE |
CUTTING EDGE SPINE, LLC |
K150321 |
02/09/2015 |
EVOS Lumbar Interbody System |
Cutting Edge Spine, LLC |
K190025 |
01/07/2019 |
EVOL« -SI Joint Fusion System |
Cutting Edge Spine, LLC |
K200552 |
03/03/2020 |
EVOS Lumbar Interbody System |
Cutting Edge Spine, LLC |
K230689 |
03/13/2023 |
T-FIXÖ 3DSI Joint Fusion System |
Cutting Edge Spine, LLC |
K180674 |
03/15/2018 |
EVOL« ha-C Cervical Interbody Fusion System |
Cutting Edge Spine, LLC |
K180891 |
04/05/2018 |
EVOL Spinal Interbody System, EVOS Lumbar Interbody System |
Cutting Edge Spine, LLC |
K200991 |
04/15/2020 |
EVOL Spinal Interbody System |
Cutting Edge Spine, LLC |
K192497 |
09/11/2019 |
EVOL ha - D Lateral Interbody Fusion System |
Cutting Edge Spine, LLC |
K214123 |
12/30/2021 |
T-FIX« 3DSI Joint Fusion System |
Cutting Edge Spine, LLC |
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