The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Biomet Modular Femoral Revision System.
Device ID | K090757 |
510k Number | K090757 |
Device Name: | BIOMET MODULAR FEMORAL REVISION SYSTEM |
Classification | Prosthesis, Hip, Semi-constrained (metal Uncemented Acetabular Component) |
Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Becky Earl |
Correspondent | Becky Earl BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | KWA |
Subsequent Product Code | JDI |
Subsequent Product Code | JDL |
Subsequent Product Code | KWY |
Subsequent Product Code | KWZ |
Subsequent Product Code | LPH |
Subsequent Product Code | LZO |
Subsequent Product Code | MAY |
Subsequent Product Code | MEH |
CFR Regulation Number | 888.3330 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2009-03-23 |
Decision Date | 2009-09-25 |
Summary: | summary |