510(k) K072989

AXIS SYSTEM by Dentsply Intl., Inc. — Product Code EFB

K072989 is an FDA 510(k) premarket notification submitted by Dentsply Intl., Inc. for the device "AXIS SYSTEM". The FDA issued a decision of Substantially Equivalent on January 28, 2008. The device falls under product code EFB (Handpiece, Air-Powered, Dental), a Class I device regulated under 21 CFR 872.4200. Dentsply Intl., Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 28, 2008
Date Received
October 23, 2007
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Handpiece, Air-Powered, Dental
Device Class
Class I
Regulation Number
872.4200
Review Panel
DE
Submission Type