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 |