The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Comprehensive Reverse Shoulder.
Device ID | K080642 |
510k Number | K080642 |
Device Name: | COMPREHENSIVE REVERSE SHOULDER |
Classification | Shoulder Prosthesis, Reverse Configuration |
Applicant | BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Contact | Patricia S Beres |
Correspondent | Patricia S Beres BIOMET, INC. 56 EAST BELL DR. BOX 587 Warsaw, IN 46581 -0587 |
Product Code | PHX |
CFR Regulation Number | 888.3660 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2008-03-06 |
Decision Date | 2008-07-09 |
Summary: | summary |