510(k) K242055

Freefix Forearm Plating System by Skeletal Dynamics, Inc. — Product Code HRS

K242055 is an FDA 510(k) premarket notification submitted by Skeletal Dynamics, Inc. for the device "Freefix Forearm Plating System". The FDA issued a decision of Substantially Equivalent on August 1, 2024. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Skeletal Dynamics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
August 1, 2024
Date Received
July 15, 2024
Clearance Type
Special
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