The following data is part of a premarket notification filed by Theken Spine Llc with the FDA for Manta Ray Anterior Cervical Plate System.
| Device ID | K080690 |
| 510k Number | K080690 |
| Device Name: | MANTA RAY ANTERIOR CERVICAL PLATE SYSTEM |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | THEKEN SPINE LLC 1800 TRIPLETT BLVD. Akron, OH 44306 |
| Contact | Dale Davison |
| Correspondent | Dale Davison THEKEN SPINE LLC 1800 TRIPLETT BLVD. Akron, OH 44306 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2008-03-11 |
| Decision Date | 2008-04-25 |
| Summary: | summary |