The following data is part of a premarket notification filed by Dentsply International, Inc. with the FDA for Ankylos Dental Implant System/claims.
| Device ID | K073067 |
| 510k Number | K073067 |
| Device Name: | ANKYLOS DENTAL IMPLANT SYSTEM/CLAIMS |
| Classification | Implant, Endosseous, Root-form |
| Applicant | DENTSPLY INTERNATIONAL, INC. SUSQUEHANNA COMMERCE CTR., 221 W. PHILADELPHIA ST., SUITE 60 York, PA 17404 |
| Contact | Helen Lewis |
| Correspondent | Helen Lewis DENTSPLY INTERNATIONAL, INC. SUSQUEHANNA COMMERCE CTR., 221 W. PHILADELPHIA ST., SUITE 60 York, PA 17404 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-30 |
| Decision Date | 2008-02-15 |
| Summary: | summary |