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 |