FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DePuy Synthes Sterilization Container System

K Number: K181933 · Decision May 9, 2019
Classifications
1
FEI Numbers
266
Registration Numbers
266
Same Product Code
279
Applicant Total
5
Review Days
294

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Basic Information

Device Name
DePuy Synthes Sterilization Container System
K Number
K181933
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 (Usa) Products, LLC / Depuy Orthopaedics, Inc.
Date Received
July 19, 2018
Decision Date
May 9, 2019
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

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (KCT), ordered by most recent decision date.

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Other Clearances by Synthes (Usa) Products, LLC / Depuy Orthopaedics, Inc.

K Number Device Name
K192745 DePuy Synthes Trauma Screws
K180310 DePuy Synthes Trauma Orthopedic Plates and Screws
K172975 DePuy Synthes (USA) 5.0mm / 7.3mm Crimp Positioning Pins – MR Conditional, DePuy Synthes Variable Angle Positioning Pins – MR Conditional, DePuy Synthes Wire Mount – MR Conditional, DePuy Synthes Cerclage Positioning Pin – MR Conditional
K160553 DePuy Synthes 4.0 mm and 5.0 mm Locking Screws – MR Conditional, DePuy Synthes Wrist Fusion Plate (WFP) – MR Conditional, DePuy Synthes Large Fragment Dynamic Compression Locking (DCL) System –MR Conditional, DePuy Synthes Small Fragment Dynamic Compression Locking (DCL) System – MR Conditional, DePuy Synthes Modular Foot System – MR Conditional, DePuy Synthes T-Plates – MR Conditional, DePuy Synthes One-third Tubular Plate with Collar (OTPC) – MR Conditional, DePuy Synthes Stainless S