The following data is part of a premarket notification filed by Zest Anchors, Inc. with the FDA for Modification To: Locator Implant Anchor.
| Device ID | K072878 |
| 510k Number | K072878 |
| Device Name: | MODIFICATION TO: LOCATOR IMPLANT ANCHOR |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | ZEST ANCHORS, INC. 2061 WINERIDGE PL. Escondido, CA 92029 |
| Contact | Richard Overton |
| Correspondent | Richard Overton ZEST ANCHORS, INC. 2061 WINERIDGE PL. Escondido, CA 92029 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2007-10-09 |
| Decision Date | 2007-12-03 |