The following data is part of a premarket notification filed by Medartis, Inc. with the FDA for Aptus Titanium Osteosynthesis System.
Device ID | K051567 |
510k Number | K051567 |
Device Name: | APTUS TITANIUM OSTEOSYNTHESIS SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | MEDARTIS, INC. 11234 EL CAMINO REAL, STE 200 San Diego, CA 92130 |
Contact | Floyd G Larson |
Correspondent | Floyd G Larson MEDARTIS, INC. 11234 EL CAMINO REAL, STE 200 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 | 2005-06-14 |
Decision Date | 2005-08-23 |
Summary: | summary |