The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Ta Interbody Fusion Device (ibd).
Device ID | K080615 |
510k Number | K080615 |
Device Name: | ENDOSKELETON TA INTERBODY FUSION DEVICE (IBD) |
Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
Applicant | TITAN SPINE, LLC 10520 BAEHR RD Mequon, WI 53092 |
Contact | Kevin Gemas |
Correspondent | Kevin Gemas TITAN SPINE, LLC 10520 BAEHR RD Mequon, WI 53092 |
Product Code | MAX |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-03-04 |
Decision Date | 2008-06-17 |
Summary: | summary |