510(k) K242486

Tyber Medical Anatomical Plating System by Tyber Medical, LLC — Product Code HRS

K242486 is an FDA 510(k) premarket notification submitted by Tyber Medical, LLC for the device "Tyber Medical Anatomical Plating System". The FDA issued a decision of Substantially Equivalent on March 19, 2025. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Tyber Medical, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
March 19, 2025
Date Received
August 21, 2024
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Plate, Fixation, Bone
Device Class
Class II
Regulation Number
888.3030
Review Panel
OR
Submission Type