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 |