The following data is part of a premarket notification filed by Biomet Manufacturing Corp. with the FDA for Maestro Wrist Plating System.
| Device ID | K110271 |
| 510k Number | K110271 |
| Device Name: | MAESTRO WRIST PLATING SYSTEM |
| Classification | Plate, Fixation, Bone |
| Applicant | BIOMET MANUFACTURING CORP. 56 BELL DRIVE Warsaw, IN 46580 |
| Contact | Patricia S Beres |
| Correspondent | Patricia S Beres BIOMET MANUFACTURING CORP. 56 BELL DRIVE Warsaw, IN 46580 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2011-01-31 |
| Decision Date | 2011-07-22 |
| Summary: | summary |