The following data is part of a premarket notification filed by Spinefrontier, Inc. with the FDA for Spinefrontier A-cift Solofuse Cervical Intervertebral Fusion Device System.
Device ID | K131880 |
510k Number | K131880 |
Device Name: | SPINEFRONTIER A-CIFT SOLOFUSE CERVICAL INTERVERTEBRAL FUSION DEVICE SYSTEM |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | SPINEFRONTIER, INC. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
Contact | Meredith May |
Correspondent | Meredith May SPINEFRONTIER, INC. 4628 NORTHPARK DRIVE Colorado Springs, CO 80918 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Abbreviated |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-06-25 |
Decision Date | 2014-01-03 |
Summary: | summary |