The following data is part of a premarket notification filed by Titan Spine, Llc with the FDA for Endoskeleton Tc.
Device ID | K100889 |
510k Number | K100889 |
Device Name: | ENDOSKELETON TC |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | TITAN SPINE, LLC 555 13TH ST, NW Washington, DC 20004 |
Contact | John J Smith |
Correspondent | John J Smith TITAN SPINE, LLC 555 13TH ST, NW Washington, DC 20004 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-03-31 |
Decision Date | 2010-07-29 |
Summary: | summary |