The following data is part of a premarket notification filed by Straumann Usa, Llc with the FDA for Straumann Cares Screw Retained Bars/bridge.
Device ID | K140737 |
510k Number | K140737 |
Device Name: | STRAUMANN CARES SCREW RETAINED BARS/BRIDGE |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | STRAUMANN USA, LLC 60 MINUTEMAN ROAD Andover, MA 01810 |
Contact | Christopher Klaczyk |
Correspondent | Christopher Klaczyk STRAUMANN USA, LLC 60 MINUTEMAN ROAD Andover, MA 01810 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2014-03-24 |
Decision Date | 2014-08-14 |
Summary: | summary |