The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Tt Interbody Fusion Device (ibd).
Device ID | K083714 |
510k Number | K083714 |
Device Name: | ENDOSKELETON TT INTERBODY FUSION DEVICE (IBD) |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
Contact | Richard Jansen |
Correspondent | Richard Jansen TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-12-15 |
Decision Date | 2009-04-15 |
Summary: | summary |