The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Arcomxl Polyethylene Liners.
Device ID | K042051 |
510k Number | K042051 |
Device Name: | ARCOMXL POLYETHYLENE LINERS |
Classification | Prosthesis, Hip, Semi-constrained, Metal/polymer, Porous Uncemented |
Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Tracy J Bickel |
Correspondent | Tracy J Bickel BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | LPH |
CFR Regulation Number | 888.3358 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2004-07-30 |
Decision Date | 2005-03-08 |
Summary: | summary |