510(k) K251296

The Acumed Wrist Fixation System by Acumed, LLC — Product Code HRS

K251296 is an FDA 510(k) premarket notification submitted by Acumed, LLC for the device "The Acumed Wrist Fixation System". The FDA issued a decision of Substantially Equivalent on June 18, 2025. The device falls under product code HRS (Plate, Fixation, Bone), a Class II device regulated under 21 CFR 888.3030. Acumed, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 18, 2025
Date Received
April 25, 2025
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