510(k) K231699

QUANTUM® Patient Specific Instrumentation (PSI) System by In2bones Sas — Product Code HSN

K231699 is an FDA 510(k) premarket notification submitted by In2bones Sas for the device "QUANTUM® Patient Specific Instrumentation (PSI) System". The FDA issued a decision of Substantially Equivalent on April 23, 2024. The device falls under product code HSN (Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer), a Class II device regulated under 21 CFR 888.3110. In2bones Sas has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 23, 2024
Date Received
June 12, 2023
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Prosthesis, Ankle, Semi-Constrained, Cemented, Metal/Polymer
Device Class
Class II
Regulation Number
888.3110
Review Panel
OR
Submission Type