The following data is part of a premarket notification filed by Implant Innovations International, Inc. with the FDA for Implant Innovation Pre-angled Abutment System.
| Device ID | K932123 |
| 510k Number | K932123 |
| Device Name: | IMPLANT INNOVATION PRE-ANGLED ABUTMENT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | IMPLANT INNOVATIONS INTERNATIONAL, INC. 3071 CONTINENTAL DR. West Palm Baeach, FL 33407 |
| Contact | William G Conety |
| Correspondent | William G Conety IMPLANT INNOVATIONS INTERNATIONAL, INC. 3071 CONTINENTAL DR. West Palm Baeach, FL 33407 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-05-03 |
| Decision Date | 1994-05-27 |