The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Ascent System.
Device ID | K982869 |
510k Number | K982869 |
Device Name: | ASCENT SYSTEM |
Classification | Prosthesis, Knee, Patellofemorotibial, Semi-constrained, Cemented, Polymer/metal/polymer |
Applicant | BIOMET, INC. P.O. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Kara Mezger |
Correspondent | Kara Mezger BIOMET, INC. P.O. BOX 587 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 | 1998-08-14 |
Decision Date | 1998-09-22 |
Summary: | summary |