The following data is part of a premarket notification filed by Implant Innovations, Inc. with the FDA for 3i Patient-specific Overdenture Bar.
| Device ID | K034035 |
| 510k Number | K034035 |
| Device Name: | 3I PATIENT-SPECIFIC OVERDENTURE BAR |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | IMPLANT INNOVATIONS, INC. 4555 RIVERSIDE DR. Palm Beach Gardens, FL 33410 |
| Contact | Jim Banic |
| Correspondent | Jim Banic IMPLANT INNOVATIONS, INC. 4555 RIVERSIDE DR. Palm Beach Gardens, FL 33410 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-12-29 |
| Decision Date | 2004-03-24 |
| Summary: | summary |