The following data is part of a premarket notification filed by Meditech Spine, Llc with the FDA for Talos Intervertebral Body Fusion Devices, Talos -c Cervical Intervertebral Body Fusion Devices, Talos -c(ha) Cervical Intervertebral Body Fusion Devices.
Device ID | K150788 |
510k Number | K150788 |
Device Name: | Talos Intervertebral Body Fusion Devices, Talos -C Cervical Intervertebral Body Fusion Devices, Talos -C(HA) Cervical Intervertebral Body Fusion Devices |
Classification | Intervertebral Fusion Device With Bone Graft, Cervical |
Applicant | MEDITECH SPINE, LLC 1447 PEACHTREE ST NE SUITE 440 Atlanta, GA 30309 |
Contact | Jason Gromek |
Correspondent | Jason Owens MEDITECH SPINE, LLC 1447 PEACHTREE ST NE SUITE 440 Atlanta, GA 30309 |
Product Code | ODP |
CFR Regulation Number | 888.3080 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2015-03-25 |
Decision Date | 2015-10-14 |
Summary: | summary |