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 |