The following data is part of a premarket notification filed by Adeor Medical Ag with the FDA for Hicut Highspeed Instrument.
Device ID | K130755 |
510k Number | K130755 |
Device Name: | HICUT HIGHSPEED INSTRUMENT |
Classification | Drills, Burrs, Trephines & Accessories (simple, Powered) |
Applicant | ADEOR MEDICAL AG KIRCHPLATZ 1 Pullach, DE 82049 |
Contact | Fabio Von Zeppelin |
Correspondent | Fabio Von Zeppelin ADEOR MEDICAL AG KIRCHPLATZ 1 Pullach, DE 82049 |
Product Code | HBE |
CFR Regulation Number | 882.4310 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-03-19 |
Decision Date | 2014-06-27 |
Summary: | summary |