510(k) K242834

System 9 Sterile Battery Container by Stryker Instruments — Product Code KCT

K242834 is an FDA 510(k) premarket notification submitted by Stryker Instruments for the device "System 9 Sterile Battery Container". The FDA issued a decision of Substantially Equivalent on January 16, 2025. The device falls under product code KCT (Sterilization Wrap Containers, Trays, Cassettes & Other Accessories), a Class II device regulated under 21 CFR 880.6850. Stryker Instruments has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
January 16, 2025
Date Received
September 19, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Sterilization Wrap Containers, Trays, Cassettes & Other Accessories
Device Class
Class II
Regulation Number
880.6850
Review Panel
HO
Submission Type