510(k) K262173

N22 Offset Humeral Head by Shoulder Innovations, Inc. — Product Code KWT

K262173 is an FDA 510(k) premarket notification submitted by Shoulder Innovations, Inc. for the device "N22 Offset Humeral Head". The FDA issued a decision of Substantially Equivalent on September 8, 2026. The device falls under product code KWT (Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented), a Class II device regulated under 21 CFR 888.3650. Shoulder Innovations, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
September 8, 2026
Date Received
June 26, 2026
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
Device Class
Class II
Regulation Number
888.3650
Review Panel
OR
Submission Type