510(k) K063512

LEKSELL GAMMA KNIFE PERFEXION by Elekta Instrument AB — Product Code IWB

K063512 is an FDA 510(k) premarket notification submitted by Elekta Instrument AB for the device "LEKSELL GAMMA KNIFE PERFEXION". The FDA issued a decision of Substantially Equivalent on March 5, 2007. The device falls under product code IWB (System, Radiation Therapy, Radionuclide), a Class II device regulated under 21 CFR 892.5750. Elekta Instrument AB has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 5, 2007
Date Received
November 20, 2006
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
System, Radiation Therapy, Radionuclide
Device Class
Class II
Regulation Number
892.5750
Review Panel
RA
Submission Type