The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Vanguard Ssk 360 Revision Knee System.
Device ID | K121149 |
510k Number | K121149 |
Device Name: | VANGUARD SSK 360 REVISION KNEE SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46581 -0587 |
Contact | Gary Baker, M.s. Rac |
Correspondent | Gary Baker, M.s. Rac BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE Warsaw, IN 46581 -0587 |
Product Code | JWH |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2012-04-16 |
Decision Date | 2012-05-16 |
Summary: | summary |