510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K042902Substantially Equivalent

Herbert Ulnar Head Prosthesis System

Stuckenbrock Medizintechnik GmbH, Miami FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K042902 is the FDA 510(k) clearance record for HERBERT ULNAR HEAD PROSTHESIS SYSTEM, a class II device, cleared for Stuckenbrock Medizintechnik GmbH on under FDA product code KXE (Prosthesis, Wrist, Hemi-, Ulnar). FDA records list 3 510(k) clearances for Stuckenbrock Medizintechnik GmbH, from to . As of , FDA records show no recalls naming K042902.

Clearance record

Decision date
Received
(68 days to decision)
Product code
KXE Prosthesis, Wrist, Hemi-, Ulnar
Regulation
21 CFR 888.3810
Device class
Class II
Review panel
Orthopedic
Applicant
Stuckenbrock Medizintechnik GmbH 12244 SW 130 St., Miami FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KXE

Trailing 12 months

FDA records hold no clearances under product code KXE in the trailing twelve months.

FDA records show no clearances under product code KXE in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KXE, 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 20260
October 20260