510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K010442Substantially Equivalent

Kurz Angular Piston-Titanium Prosthesis, Models 1006 600, 1006 601, 1006 602, 1006 650, 1006 651, 1006 652

Heinz Kurz, Amsterdam 1017ap, NL / Special, Substantially Equivalent
FDA source (opens on fda.gov)

K010442 is the FDA 510(k) clearance record for KURZ ANGULAR PISTON-TITANIUM PROSTHESIS, MODELS 1006 600, 1006 601, 1006 602, 1006 650, 1006 651, 1006 652, a class II device, cleared for Heinz Kurz on under FDA product code ETB (Prosthesis, Partial Ossicular Replacement). FDA records list 5 510(k) clearances for Heinz Kurz, from to . As of , FDA records show no recalls naming K010442.

Clearance record

Decision date
Received
(22 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
Heinz Kurz Amstel 320-I, Amsterdam 1017ap, NL
510(k) summary
Summary
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