The following data is part of a premarket notification filed by Medtronic Xomed, Inc. with the FDA for Ipc Powerease System.
| Device ID | K111520 | 
| 510k Number | K111520 | 
| Device Name: | IPC POWEREASE SYSTEM | 
| Classification | Drills, Burrs, Trephines & Accessories (simple, Powered) | 
| Applicant | MEDTRONIC XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 | 
| Contact | Rishi Sinha | 
| Correspondent | Rishi Sinha MEDTRONIC XOMED, INC. 6743 SOUTHPOINT DR. NORTH Jacksonville, FL 32216 | 
| Product Code | HBE | 
| Subsequent Product Code | GWF | 
| Subsequent Product Code | HWE | 
| CFR Regulation Number | 882.4310 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2011-06-02 | 
| Decision Date | 2011-10-26 | 
| Summary: | summary |