The following data is part of a premarket notification filed by Titan Implants with the FDA for O-ring Prosthetic Attachment.
| Device ID | K001638 | 
| 510k Number | K001638 | 
| Device Name: | O-RING PROSTHETIC ATTACHMENT | 
| Classification | Implant, Endosseous, Root-form | 
| Applicant | TITAN IMPLANTS 203 MAIN STREET, PMB 166 Flemington, NJ 08822 | 
| Contact | Lynette L Howard | 
| Correspondent | Lynette L Howard TITAN IMPLANTS 203 MAIN STREET, PMB 166 Flemington, NJ 08822  | 
| Product Code | DZE | 
| CFR Regulation Number | 872.3640 [🔎] | 
| Decision | Substantially Equivalent (SESE) | 
| Type | Traditional | 
| 3rd Party Reviewed | No | 
| Combination Product | No | 
| Date Received | 2000-05-30 | 
| Decision Date | 2002-03-04 |