The following data is part of a premarket notification filed by Titan Spine, Inc with the FDA for Endoskeleton Tl Interbody Fusion Device, Endoskeleton Tl Hyperlordotic Interbody Fusion Device.
Device ID | K191581 |
510k Number | K191581 |
Device Name: | Endoskeleton TL Interbody Fusion Device, Endoskeleton TL Hyperlordotic Interbody Fusion Device |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | Titan Spine, Inc 6140 W. Executive Dr., Suite A Mequon, WI 53092 |
Contact | Kelly Mcdonnell |
Correspondent | Christine Scifert Mrc/x, Llc 6075 Poplar Avenue Memphis, TN 38119 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2019-06-14 |
Decision Date | 2020-01-08 |