510(k) K082637

CRANIAL PERFORATOR by The Anspach Effort, Inc. — Product Code HBF

K082637 is an FDA 510(k) premarket notification submitted by The Anspach Effort, Inc. for the device "CRANIAL PERFORATOR". The FDA issued a decision of Substantially Equivalent on December 22, 2008. The device falls under product code HBF (Drills, Burrs, Trephines & Accessories (Compound, Powered)), a Class II device regulated under 21 CFR 882.4305. The Anspach Effort, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
December 22, 2008
Date Received
September 10, 2008
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