510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K241261Substantially Equivalent

mCLIP Partial Prosthesis, mCLIP ARC Partial Prosthesis, mXACT Partial Prosthesis and mXACT PRO Partial Prosthesis Kit

MED-EL Elektromedizinische Geräte GmbH, Innsbruck, AT / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K241261 is the FDA 510(k) clearance record for mCLIP Partial Prosthesis, mCLIP ARC Partial Prosthesis, mXACT Partial Prosthesis and mXACT PRO Partial Prosthesis Kit, a class II device, cleared for MED-EL Elektromedizinische Geräte GmbH on under FDA product code ETB (Prosthesis, Partial Ossicular Replacement). FDA records list 6 510(k) clearances for MED-EL Elektromedizinische Geräte GmbH, from to . As of , FDA records show no recalls naming K241261.

Clearance record

Decision date
Received
(266 days to decision)
Product code
ETB Prosthesis, Partial Ossicular Replacement
Regulation
21 CFR 874.3450
Device class
Class II
Review panel
Ear, Nose, Throat
Applicant
MED-EL Elektromedizinische Geräte GmbH Fürstenweg 77a, Innsbruck, AT
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ETB

Trailing 12 months
2 clearances under product code ETB in the twelve months to October 2026, April 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code ETB, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20262
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260