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 |