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 |