The following data is part of a premarket notification filed by Medtronic Sofamor Danek Usa, Inc. with the FDA for Artic-l 3d Ti Spinal System With Tionic Technology, Artic-xl 3d Ti Spinal System With Tionic Technology.
Device ID | K171689 |
510k Number | K171689 |
Device Name: | ARTiC-L 3D Ti Spinal System With TiONIC Technology, ARTiC-XL 3D Ti Spinal System With TiONIC Technology |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place Memphis, TN 38132 |
Contact | Kelly Anglin |
Correspondent | Tejas Patel Medtronic Sofamor Danek USA, Inc. 1800 Pyramid Place Memphis, TN 38132 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2017-06-07 |
Decision Date | 2017-10-05 |
Summary: | summary |