The following data is part of a premarket notification filed by Core-vent Corp. with the FDA for Advent Implant System.
| Device ID | K002614 |
| 510k Number | K002614 |
| Device Name: | ADVENT IMPLANT SYSTEM |
| Classification | Implant, Endosseous, Root-form |
| Applicant | CORE-VENT CORP. 4630 SOUTH ARVILLE STE D Las Vegas, NV 89103 |
| Contact | Will Fisher |
| Correspondent | Will Fisher CORE-VENT CORP. 4630 SOUTH ARVILLE STE D Las Vegas, NV 89103 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2000-08-22 |
| Decision Date | 2000-12-08 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00889024020245 | K002614 | 000 |
| 00889024013858 | K002614 | 000 |
| 00889024013841 | K002614 | 000 |
| 00889024014855 | K002614 | 000 |
| 00889024014848 | K002614 | 000 |
| 00889024014138 | K002614 | 000 |
| 00889024014121 | K002614 | 000 |
| 00889024014114 | K002614 | 000 |
| 00889024014107 | K002614 | 000 |
| 00889024014039 | K002614 | 000 |
| 00889024013926 | K002614 | 000 |
| 00889024013896 | K002614 | 000 |
| 00889024013889 | K002614 | 000 |
| 00889024013872 | K002614 | 000 |
| 00889024013902 | K002614 | 000 |
| 00889024013933 | K002614 | 000 |
| 00889024014091 | K002614 | 000 |
| 00889024014077 | K002614 | 000 |
| 00889024014053 | K002614 | 000 |
| 00889024014046 | K002614 | 000 |
| 00889024014022 | K002614 | 000 |
| 00889024014015 | K002614 | 000 |
| 00889024014008 | K002614 | 000 |
| 00889024013995 | K002614 | 000 |
| 00889024013988 | K002614 | 000 |
| 00889024013971 | K002614 | 000 |
| 00889024013964 | K002614 | 000 |
| 00889024013957 | K002614 | 000 |
| 00889024013940 | K002614 | 000 |
| 00889024013865 | K002614 | 000 |