The following data is part of a premarket notification filed by Medartis Ag with the FDA for Aptus Wrist Spanning Plates 2.5.
Device ID | K191848 |
510k Number | K191848 |
Device Name: | APTUS Wrist Spanning Plates 2.5 |
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 | 2019-07-10 |
Decision Date | 2019-09-30 |
Summary: | summary |