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 |