OsteoMed ExtremiFix Mini & Small System Tray

FDA 510(k) K202105 · Osteomed, LLC

Substantially Equivalent

510(k) numberK202105

Submission

Device name
OsteoMed ExtremiFix Mini & Small System Tray
Applicant
Osteomed, LLC
Addison, TX, US
Received
July 29, 2020
Decision date
October 29, 2020
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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K161041OsteoMed ExtremiLOCK Wrist Plating SystemHRS · Special 05/19/2016SE
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Questions and answers

When was OsteoMed ExtremiFix Mini & Small System Tray cleared by the FDA?

OsteoMed ExtremiFix Mini & Small System Tray (K202105) received a 510(k) decision of Substantially Equivalent on October 29, 2020, 92 days after the submission was received.

What is the product code of K202105?

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.