The following data is part of a premarket notification filed by Biohorizons Implant Systems, Inc. with the FDA for Biohorizons Abutments For Zimmer.
Device ID | K103691 |
510k Number | K103691 |
Device Name: | BIOHORIZONS ABUTMENTS FOR ZIMMER |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | BIOHORIZONS IMPLANT SYSTEMS, INC. 2300 RIVERCHASE CENTER Birmingham, AL 35244 |
Contact | Michael Davis |
Correspondent | Michael Davis BIOHORIZONS IMPLANT SYSTEMS, INC. 2300 RIVERCHASE CENTER Birmingham, AL 35244 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-12-17 |
Decision Date | 2011-11-03 |
Summary: | summary |