FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇭 Switzerland

Hoffmann LRF System

K Number: K253202 · Decision Dec 19, 2025
Classifications
1
FEI Numbers
249
Registration Numbers
249
Same Product Code
403
Applicant Total
54
Review Days
84

Basic Information

Device Name
Hoffmann LRF System
K Number
K253202
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker GmbH
Date Received
September 26, 2025
Decision Date
December 19, 2025
Product Code
KTT
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
KTT Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component

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