OsteoMed QuickFix Hybrid MMF Sterilization Tray
K-Number: K173391 · 2018-05-10
ApplicantOsteomed, LLC
Decision Date2018-05-10
Product CodeKCT
Advisory CommitteeHO
DecisionSubstantially Equivalent
Device Summary
OsteoMed QuickFix Hybrid MMF Sterilization Tray is a medical device manufactured by Osteomed, LLC. It received FDA 510(k) clearance on 2018-05-10 under approval number K173391. The device is classified under product code KCT. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the OsteoMed QuickFix Hybrid MMF Sterilization Tray?
OsteoMed QuickFix Hybrid MMF Sterilization Tray is a medical device that received FDA 510(k) clearance on 2018-05-10. It is manufactured by Osteomed, LLC. The 510(k) number is K173391.
When was OsteoMed QuickFix Hybrid MMF Sterilization Tray approved by the FDA?
OsteoMed QuickFix Hybrid MMF Sterilization Tray received FDA 510(k) clearance on 2018-05-10, under approval number K173391.
What company makes OsteoMed QuickFix Hybrid MMF Sterilization Tray?
OsteoMed QuickFix Hybrid MMF Sterilization Tray is manufactured by Osteomed, LLC.
What is the FDA product code for OsteoMed QuickFix Hybrid MMF Sterilization Tray?
The FDA product code for OsteoMed QuickFix Hybrid MMF Sterilization Tray is KCT.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.