The following data is part of a premarket notification filed by Soadco S.l. with the FDA for Klockner Vega Tibase For Cerec.
| Device ID | K170022 |
| 510k Number | K170022 |
| Device Name: | Klockner Vega TiBase For CEREC |
| Classification | Abutment, Implant, Dental, Endosseous |
| Applicant | SOADCO S.L. AVGDA. FITER I ROSELLL, 4 BIS - LOCAL 2 Escaldes - Engordany, AD Ad-700 |
| Contact | Maria Mitjaneta |
| Correspondent | Maria Mitjaneta SOADCO S.L. AVGDA. FITER I ROSELLL, 4 BIS - LOCAL 2 Escaldes - Engordany, AD Ad-700 |
| Product Code | NHA |
| CFR Regulation Number | 872.3630 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Abbreviated |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2017-01-03 |
| Decision Date | 2017-11-16 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 08435451602855 | K170022 | 000 |
| 08435451602831 | K170022 | 000 |
| 08435451602794 | K170022 | 000 |
| 08435451647092 | K170022 | 000 |
| 08435451646910 | K170022 | 000 |
| 08435451646552 | K170022 | 000 |