510(k) K090676

MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES by Anthogyr — Product Code EFA

K090676 is an FDA 510(k) premarket notification submitted by Anthogyr for the device "MONTBLANC IMPLANTOLOGY AND OMNIPRATIQUE CONTRA-ANGLES". The FDA issued a decision of Substantially Equivalent on May 22, 2009. The device falls under product code EFA (Handpiece, Belt And/Or Gear Driven, Dental), a Class I device regulated under 21 CFR 872.4200. Anthogyr has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
May 22, 2009
Date Received
March 13, 2009
Clearance Type
Special
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Handpiece, Belt And/Or Gear Driven, Dental
Device Class
Class I
Regulation Number
872.4200
Review Panel
DE
Submission Type