The following data is part of a premarket notification filed by Soadco, S.l. with the FDA for Klockner Dental Implants, Models Sk, Nk, Ik, S3, And S4.
| Device ID | K010132 |
| 510k Number | K010132 |
| Device Name: | KLOCKNER DENTAL IMPLANTS, MODELS SK, NK, IK, S3, AND S4 |
| Classification | Implant, Endosseous, Root-form |
| Applicant | SOADCO, S.L. AV FITER I ROSSELL 4 BIS LOCAL 2 Escaldes-engordany, AD Ad-700 |
| Contact | Mercedes Roldan |
| Correspondent | Mercedes Roldan SOADCO, S.L. AV FITER I ROSSELL 4 BIS LOCAL 2 Escaldes-engordany, AD Ad-700 |
| Product Code | DZE |
| CFR Regulation Number | 872.3640 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2001-01-16 |
| Decision Date | 2002-06-04 |