510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K140961Substantially Equivalent

Hoffmann Lrf (Limb Reconstruction Frame) System

Stryker Trauma GmbH, Selzach, CH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K140961 is the FDA 510(k) clearance record for HOFFMANN LRF (LIMB RECONSTRUCTION FRAME) SYSTEM, a class II device, cleared for Stryker Trauma AG on under FDA product code KTT (Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component). FDA records list 32 510(k) clearances for Stryker Trauma AG, from to . As of , FDA records show no recalls naming K140961.

Clearance record

Decision date
Received
(209 days to decision)
Product code
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
Regulation
21 CFR 888.3030
Device class
Class II
Review panel
Orthopedic
Applicant
Stryker Trauma AG Bohnackerweg 1, Selzach, CH
510(k) summary
Summary PDF
Third party review
No

Clearances, product code KTT

Trailing 12 months
8 clearances under product code KTT in the twelve months to October 2026, November 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code KTT, trailing twelve months
MonthClearances
November 20252
December 20252
January 20261
February 20260
March 20261
April 20261
May 20260
June 20261
July 20260
August 20260
September 20260
October 20260