The following data is part of a premarket notification filed by Medartis Ag with the FDA for Aptus Wrist 2.5 System.
| Device ID | K142906 |
| 510k Number | K142906 |
| Device Name: | APTUS Wrist 2.5 System |
| Classification | Plate, Fixation, Bone |
| Applicant | MEDARTIS AG HOCHBERGERSTRASSE 60E Basel, CH Ch-4057 |
| Contact | Andrea Schweizer |
| Correspondent | Kevin A Thomas PAXMED INTERNATIONAL, LLC 12264 EL CAMINO REAL SUITE 400 San Diego, CA 92130 |
| Product Code | HRS |
| CFR Regulation Number | 888.3030 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2014-10-06 |
| Decision Date | 2015-06-09 |
| Summary: | summary |