510(k) K892866

AUTOMATIC CRANIAL DRILL (PERFORATOR) by Acra Cut, Inc. — Product Code HBF

K892866 is an FDA 510(k) premarket notification submitted by Acra Cut, Inc. for the device "AUTOMATIC CRANIAL DRILL (PERFORATOR)". The FDA issued a decision of Substantially Equivalent on June 15, 1989. The device falls under product code HBF (Drills, Burrs, Trephines & Accessories (Compound, Powered)), a Class II device regulated under 21 CFR 882.4305. Acra Cut, Inc. has at least 7 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 15, 1989
Date Received
April 19, 1989
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Drills, Burrs, Trephines & Accessories (Compound, Powered)
Device Class
Class II
Regulation Number
882.4305
Review Panel
NE
Submission Type