510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K943635Substantially Equivalent

Ultra-Line Rongeur

V. Mueller Neuro/Spine, San Carlos CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K943635 is the FDA 510(k) clearance record for ULTRA-LINE RONGEUR, a class II device, cleared for V. Mueller Neuro/Spine on under FDA product code HAE (Rongeur, Manual). FDA records list 8 510(k) clearances for V. Mueller Neuro/Spine, from to . As of , FDA records show no recalls naming K943635.

Clearance record

Decision date
Received
(133 days to decision)
Product code
HAE Rongeur, Manual
Regulation
21 CFR 882.4840
Device class
Class II
Review panel
Neurology
Applicant
V. Mueller Neuro/Spine 871 Industrial Rd., San Carlos CA
510(k) summary
Statement
Third party review
No

Clearances, product code HAE

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