OsteoMed QuickFix Hybrid MMF Sterilization Tray

FDA 510(k) K173391 · Osteomed, LLC

Substantially Equivalent

510(k) numberK173391

Submission

Device name
OsteoMed QuickFix Hybrid MMF Sterilization Tray
Applicant
Osteomed, LLC
Addison, TX, US
Received
October 30, 2017
Decision date
May 10, 2018
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device class
Class II (moderate risk)
Regulation
21 CFR 880.6850
Specialty
General Hospital

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Questions and answers

When was OsteoMed QuickFix Hybrid MMF Sterilization Tray cleared by the FDA?

OsteoMed QuickFix Hybrid MMF Sterilization Tray (K173391) received a 510(k) decision of Substantially Equivalent on May 10, 2018, 192 days after the submission was received.

What is the product code of K173391?

The FDA product code is KCT – Sterilization Wrap Containers, Trays, Cassettes & Other Accessories, a Class II (moderate risk) device regulated under 21 CFR 880.6850.