510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K213135Substantially Equivalent

Plasma Edge resection and vaporization electrodes, Plasma Edge working elements, Adaptor Plasma Edge

Chirurgie Innovation, Verrières Le Buisson, FR / Special, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K213135 is the FDA 510(k) clearance record for Plasma Edge resection and vaporization electrodes, Plasma Edge working elements, Adaptor Plasma Edge, a class II device, cleared for Chirurgie Innovation on under FDA product code FAS (Electrode, Electrosurgical, Active, Urological). FDA records list 2 510(k) clearances for Chirurgie Innovation, from to . As of , FDA records show no recalls naming K213135.

Clearance record

Decision date
Received
(156 days to decision)
Product code
FAS Electrode, Electrosurgical, Active, Urological
Regulation
21 CFR 876.4300
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Chirurgie Innovation Z.A Les Godets, 3 Rue Des Petits Ruisseaux, Verrières Le Buisson, FR
510(k) summary
Summary PDF
Third party review
No

Clearances, product code FAS

Trailing 12 months
1 clearance under product code FAS in the twelve months to October 2026, December 2025 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code FAS, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260