510(k) K242834

Device
System 9 Sterile Battery Container
Applicant
Stryker Instruments
510(k) number
K242834
Product code
KCT
Decision
Substantially Equivalent (SESE)
Decision date
2025-01-16
Date received
2024-09-19
Regulation
880.6850
Classification name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Medical specialty
General Hospital
Review panel
General Hospital
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
N
Source
FDA openFDA 510(k) dataset plus migrated FDA.report data

Related Records

Applicant Contact

Contact
Megan Guilbault
Address
1941 Stryker Way Portage MI US 49002 49002

FDA Registration Numbers

Source Documents

FDA 510(k) Premarket Notification Database · 510(k) summary PDF · openFDA JSON

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