510(k) K241817

InSet Total Shoulder System by Shoulder Innovations, Inc. — Product Code KWT

K241817 is an FDA 510(k) premarket notification submitted by Shoulder Innovations, Inc. for the device "InSet Total Shoulder System". The FDA issued a decision of Substantially Equivalent on February 11, 2025. 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
February 11, 2025
Date Received
June 24, 2024
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