The following data is part of a premarket notification filed by Anthogyr Sas with the FDA for Anthogyr Implanteo Implantology And Dental Surgical Motor Unit.
Device ID | K102241 |
510k Number | K102241 |
Device Name: | ANTHOGYR IMPLANTEO IMPLANTOLOGY AND DENTAL SURGICAL MOTOR UNIT |
Classification | Controller, Foot, Handpiece And Cord |
Applicant | ANTHOGYR SAS 2237, AVENUE ANDRE LASQUIN Sallanches, FR 74700 |
Contact | Brayette Sabine |
Correspondent | Brayette Sabine ANTHOGYR SAS 2237, AVENUE ANDRE LASQUIN Sallanches, FR 74700 |
Product Code | EBW |
CFR Regulation Number | 872.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-08-09 |
Decision Date | 2011-03-23 |
Summary: | summary |