510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K132044Substantially Equivalent

Cranial Loop, Cranial Loop L and Cranial Loop Xl and Cranial Bone Fixation System

Neos Surgery S.L., Alexandria VA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K132044 is the FDA 510(k) clearance record for CRANIAL LOOP, CRANIAL LOOP L AND CRANIAL LOOP XL AND CRANIAL BONE FIXATION SYSTEM, a class II device, cleared for Neos Surgery S.L on under FDA product code GXR (Cover, Burr Hole). FDA records list 6 510(k) clearances for Neos Surgery S.L, from to . As of , FDA records show no recalls naming K132044.

Clearance record

Decision date
Received
(90 days to decision)
Product code
GXR Cover, Burr Hole
Regulation
21 CFR 882.5250
Device class
Class II
Review panel
Neurology
Applicant
Neos Surgery S.L 901 King St., Suite 101, Alexandria VA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code GXR

Trailing 12 months
1 clearance under product code GXR in the twelve months to October 2026, March 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code GXR, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20261
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260