CRANIOCUT


Device Classification Name

drills, burrs, trephines & accessories (simple, powered)

510(k) Number K022942
Device Name CRANIOCUT
Original Applicant
AESCULAP, INC.
3773 corporate parkway
center valley, 
PA 
18034

Original Contact georg keller
Regulation Number 882.4310
Classification Product Code
HBE  
Date Received 09/05/2002
Decision Date 10/21/2002
Decision

substantially equivalent

(SESE)

Regulation Medical Specialty

Neurology

510k Review Panel

Neurology

summary

summary

Type Traditional
Reviewed by Third Party No

Combination Product

No