The following data is part of a premarket notification filed by Amedica Corp. with the FDA for Valeo Cervical Plate System.
| Device ID | K071990 |
| 510k Number | K071990 |
| Device Name: | VALEO CERVICAL PLATE SYSTEM |
| Classification | Appliance, Fixation, Spinal Intervertebral Body |
| Applicant | AMEDICA CORP. 1331 H ST. NW, 12TH FLOOR Washington, DC 20005 |
| Contact | Glenn Stiegman |
| Correspondent | Glenn Stiegman AMEDICA CORP. 1331 H ST. NW, 12TH FLOOR Washington, DC 20005 |
| Product Code | KWQ |
| CFR Regulation Number | 888.3060 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-07-20 |
| Decision Date | 2007-10-29 |
| Summary: | summary |