The following data is part of a premarket notification filed by Innova Corp. with the FDA for Hybrid Endopore Endosseous Dental Implant.
| Device ID | K040714 |
| 510k Number | K040714 |
| Device Name: | HYBRID ENDOPORE ENDOSSEOUS DENTAL IMPLANT |
| Classification | Implant, Endosseous, Root-form |
| Applicant | INNOVA CORP. C/O HOGAN & HARTSON 555 THIRTEENTH STREET, N.W. Washington, DC 20004 |
| Contact | Howard Holstein |
| Correspondent | Howard Holstein INNOVA CORP. C/O HOGAN & HARTSON 555 THIRTEENTH STREET, N.W. Washington, DC 20004 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2004-03-18 |
| Decision Date | 2004-04-09 |
| Summary: | summary |