510(k) K242436

Proximal Humerus Fixation System by Skeletal Dynamics, Inc. — Product Code HRS

K242436 is an FDA 510(k) premarket notification submitted by Skeletal Dynamics, Inc. for the device "Proximal Humerus Fixation System". The FDA issued a decision of Substantially Equivalent on November 14, 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
November 14, 2024
Date Received
August 16, 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