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

Synthes Graphic Case & Tray System

K Number: K241927 · Decision Mar 28, 2025
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
7
Review Days
270

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Basic Information

Device Name
Synthes Graphic Case & Tray System
K Number
K241927
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.6850
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Synthes GmbH
Date Received
July 1, 2024
Decision Date
March 28, 2025
Product Code
KCT
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
KCT Sterilization Wrap Containers, Trays, Cassettes & Other Accessories

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K254054 VOLT™ Ankle Trauma 2.7/3.5 Plating System; VOLT™ Calcaneus 2.7 Plating System
K243715 Synthes Patient Specific Implants
K233994 VOLT™ Proximal Humerus 3.5 Plating System
K233967 DePuy Synthes MatrixSTERNUM Fixation System