510(k) K252416

AETOS Shoulder System Meta Humeral Prosthesis Size 0 by Smith & Nephew, Inc. — Product Code KWS

K252416 is an FDA 510(k) premarket notification submitted by Smith & Nephew, Inc. for the device "AETOS Shoulder System Meta Humeral Prosthesis Size 0". The FDA issued a decision of Substantially Equivalent on October 29, 2025. The device falls under product code KWS (Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented), a Class II device regulated under 21 CFR 888.3660. Smith & Nephew, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
October 29, 2025
Date Received
August 1, 2025
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Device Class
Class II
Regulation Number
888.3660
Review Panel
OR
Submission Type