The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Tcs System.
Device ID | K142940 |
510k Number | K142940 |
Device Name: | Endoskeleton TCS System |
Classification | Intervertebral Fusion Device With Integrated Fixation, Cervical |
Applicant | TITAN SPINE, LLC 6140 WEST EXECUTIVE DRIVE, SUITE A Mequon, WI 53092 |
Contact | Jane Rodd |
Correspondent | Christine Scifert MEMPHIS REGULATORY CONSULTING, LLC 3416 ROXEE RUN COVE Bartlette, TN 38133 |
Product Code | OVE |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-10-09 |
Decision Date | 2015-01-28 |
Summary: | summary |