510(k) K250536

MetaFore Small Screw System by Extremity Medical, LLC — Product Code HWC

K250536 is an FDA 510(k) premarket notification submitted by Extremity Medical, LLC for the device "MetaFore Small Screw System". The FDA issued a decision of Substantially Equivalent on October 8, 2025. The device falls under product code HWC (Screw, Fixation, Bone), a Class II device regulated under 21 CFR 888.3040. Extremity Medical, LLC has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 8, 2025
Date Received
February 24, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Screw, Fixation, Bone
Device Class
Class II
Regulation Number
888.3040
Review Panel
OR
Submission Type