The following data is part of a premarket notification filed by Biohorizons Implant Systems, Inc. with the FDA for Multi-unit Abutments For Conelog.
Device ID | K203252 |
510k Number | K203252 |
Device Name: | Multi-unit Abutments For CONELOG |
Classification | Abutment, Implant, Dental, Endosseous |
Applicant | BioHorizons Implant Systems, Inc. 2300 Riverchase Center Birmingham, AL 35244 |
Contact | Bill Hornbuckle |
Correspondent | Floyd G Larson PaxMed International, LLC 12264 El Camino Real, Suite 400 San Diego, CA 92130 |
Product Code | NHA |
CFR Regulation Number | 872.3630 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-11-04 |
Decision Date | 2021-03-16 |
Summary: | summary |
Device Identifier | submissionNumber | Supplement |
---|---|---|
00847236015459 | K203252 | 000 |
00847236015268 | K203252 | 000 |
00847236015251 | K203252 | 000 |
00847236015244 | K203252 | 000 |
00847236015237 | K203252 | 000 |
00847236015220 | K203252 | 000 |
00847236015213 | K203252 | 000 |
00847236015206 | K203252 | 000 |
00847236015190 | K203252 | 000 |
00847236015183 | K203252 | 000 |
00847236015176 | K203252 | 000 |
00847236015169 | K203252 | 000 |
00847236021771 | K203252 | 000 |
00847236021764 | K203252 | 000 |
00847236021757 | K203252 | 000 |
00847236021740 | K203252 | 000 |
00847236021733 | K203252 | 000 |
00847236015275 | K203252 | 000 |
00847236015282 | K203252 | 000 |
00847236015442 | K203252 | 000 |
00847236015435 | K203252 | 000 |
00847236015428 | K203252 | 000 |
00847236015411 | K203252 | 000 |
00847236015404 | K203252 | 000 |
00847236015398 | K203252 | 000 |
00847236015381 | K203252 | 000 |
00847236015374 | K203252 | 000 |
00847236015367 | K203252 | 000 |
00847236015350 | K203252 | 000 |
00847236015343 | K203252 | 000 |
00847236015336 | K203252 | 000 |
00847236015329 | K203252 | 000 |
00847236015312 | K203252 | 000 |
00847236015305 | K203252 | 000 |
00847236015299 | K203252 | 000 |
00847236021726 | K203252 | 000 |