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 |