The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton(r) Tas.
Device ID | K111626 |
510k Number | K111626 |
Device Name: | ENDOSKELETON(R) TAS |
Classification | Intervertebral Fusion Device With Integrated Fixation, Lumbar |
Applicant | TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
Contact | Rich Jansen |
Correspondent | Rich Jansen TITAN SPINE, LLC 13540 GUILD AVE Apple Valley, MN 55124 |
Product Code | OVD |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-06-10 |
Decision Date | 2011-09-09 |
Summary: | summary |