The following data is part of a premarket notification filed by Amedica Corp. with the FDA for Phantom Plus Ceramic Cage System.
| Device ID | K121892 |
| 510k Number | K121892 |
| Device Name: | PHANTOM PLUS CERAMIC CAGE SYSTEM |
| Classification | Intervertebral Fusion Device With Bone Graft, Lumbar |
| Applicant | AMEDICA CORP. 615 ARAPEEN DRIVE Salt Lake City, UT 84108 |
| Contact | Robert M Wolfarth |
| Correspondent | Robert M Wolfarth AMEDICA CORP. 615 ARAPEEN DRIVE Salt Lake City, UT 84108 |
| Product Code | MAX |
| CFR Regulation Number | 888.3080 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2012-06-29 |
| Decision Date | 2012-08-24 |
| Summary: | summary |