The following data is part of a premarket notification filed by Spinecraft, Inc. with the FDA for Apex Spine System.
Device ID | K062513 |
510k Number | K062513 |
Device Name: | APEX SPINE SYSTEM |
Classification | Appliance, Fixation, Spinal Interlaminal |
Applicant | SPINECRAFT, INC. 2215 ENTERPRISE DRIVE SUITE 1504 Westchester, IL 60154 |
Contact | Ami Akallal-asaad |
Correspondent | Ami Akallal-asaad SPINECRAFT, INC. 2215 ENTERPRISE DRIVE SUITE 1504 Westchester, IL 60154 |
Product Code | KWP |
Subsequent Product Code | KWQ |
Subsequent Product Code | MNH |
Subsequent Product Code | MNI |
CFR Regulation Number | 888.3050 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2006-08-28 |
Decision Date | 2006-12-22 |
Summary: | summary |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
APEX SPINE SYSTEM 85820194 not registered Dead/Abandoned |
SpineCraft, LLC 2013-01-10 |