The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Vanguard Complete Knee System.
Device ID | K113550 |
510k Number | K113550 |
Device Name: | VANGUARD COMPLETE KNEE SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Gary Baker |
Correspondent | Gary Baker BIOMET MANUFACTURING CORP. 56 EAST BELL DRIVE P.O. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | JWH |
Subsequent Product Code | MBH |
Subsequent Product Code | OIY |
CFR Regulation Number | 888.3560 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-12-01 |
Decision Date | 2012-02-29 |
Summary: | summary |