The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Rx90 Low Profile Acetabular System.
Device ID | K042989 |
510k Number | K042989 |
Device Name: | RX90 LOW PROFILE ACETABULAR SYSTEM |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Patricia Sandborn Beres |
Correspondent | Patricia Sandborn Beres BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | LPH |
Subsequent Product Code | JDI |
Subsequent Product Code | KWZ |
Subsequent Product Code | LZO |
Subsequent Product Code | MEH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-10-29 |
Decision Date | 2005-04-28 |
Summary: | summary |