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 |