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 |