The following data is part of a premarket notification filed by Implant Innovations International, Inc. with the FDA for Overdenture Attachment.
Device ID | K891613 |
510k Number | K891613 |
Device Name: | OVERDENTURE ATTACHMENT |
Classification | Implant, Endosseous, Root-form |
Applicant | IMPLANT INNOVATIONS INTERNATIONAL, INC. 1897 PALM BEACH LAKES BLVD. SUITE 114 West Palm Beach, FL 33409 |
Contact | J Lazzara |
Correspondent | J Lazzara IMPLANT INNOVATIONS INTERNATIONAL, INC. 1897 PALM BEACH LAKES BLVD. SUITE 114 West Palm Beach, FL 33409 |
Product Code | DZE |
CFR Regulation Number | 872.3640 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-03-20 |
Decision Date | 1989-10-10 |