510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K913619Substantially Equivalent

Ceravital Middle Ear Implant

Friedrichsfeld Medizintechnik AG, Walnut Creek CA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913619 is the FDA 510(k) clearance record for CERAVITAL MIDDLE EAR IMPLANT, a class II device, cleared for Friedrichsfeld Medizintechnik AG on under FDA product code ETB (Prosthesis, Partial Ossicular Replacement). FDA records list one 510(k) clearance for Friedrichsfeld Medizintechnik AG. As of , FDA records show no recalls naming K913619.

Clearance record

Decision date
Received
(63 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
Friedrichsfeld Medizintechnik AG 47 Quail Ct., Walnut Creek CA
510(k) summary
Statement
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