510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K073018Substantially Equivalent

Stereotactic Target Positioner, Target Positioner for Leksell Headring, Stereotactic Counterweight

Brainlab, Inc., Feldkirchen, DE / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K073018 is the FDA 510(k) clearance record for STEREOTACTIC TARGET POSITIONER, TARGET POSITIONER FOR LEKSELL HEADRING, STEREOTACTIC COUNTERWEIGHT, a class II device, cleared for Brainlab AG on under FDA product code IYE (Accelerator, Linear, Medical). FDA records list 146 510(k) clearances for Brainlab AG, from to . As of , FDA records show one recall naming K073018.

Clearance record

Decision date
Received
(90 days to decision)
Product code
IYE Accelerator, Linear, Medical
Regulation
21 CFR 892.5050
Device class
Class II
Review panel
Radiology
Applicant
Brainlab AG Kapellenstrasse 12, Feldkirchen, DE
510(k) summary
Summary PDF
Third party review
No

Clearances, product code IYE

Trailing 12 months
16 clearances under product code IYE in the twelve months to October 2026, January 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code IYE, trailing twelve months
MonthClearances
November 20251
December 20251
January 20264
February 20260
March 20261
April 20262
May 20261
June 20262
July 20260
August 20263
September 20261
October 20260