The following data is part of a premarket notification filed by Medartis Ag with the FDA for Aptus Cannulated Compression Screws.
Device ID | K133460 |
510k Number | K133460 |
Device Name: | APTUS CANNULATED COMPRESSION SCREWS |
Classification | Screw, Fixation, Bone |
Applicant | MEDARTIS AG 12264 EL CAMINO REAL, STE 400 San Diego, CA 92130 |
Contact | Allison Komiyama |
Correspondent | Allison Komiyama MEDARTIS AG 12264 EL CAMINO REAL, STE 400 San Diego, CA 92130 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2013-11-12 |
Decision Date | 2013-12-18 |
Summary: | summary |