The following data is part of a premarket notification filed by Biomet, Inc. with the FDA for Comprehensive Segmental Revision System (srs).
Device ID | K111746 |
510k Number | K111746 |
Device Name: | COMPREHENSIVE SEGMENTAL REVISION SYSTEM (SRS) |
Classification | Prosthesis, Shoulder, Non-constrained, Metal/polymer Cemented |
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 | KWT |
Subsequent Product Code | JDC |
Subsequent Product Code | KWS |
Subsequent Product Code | MBF |
CFR Regulation Number | 888.3650 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-06-21 |
Decision Date | 2011-12-15 |
Summary: | summary |