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CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C); CrossWise RF Adapter Cable (Model CW-1002)

K241414 Class II Traditional
Decision Date
2024-09-26
Sponsor / Applicant
Circa Scientific, Inc.

Technical Specification

510(k) Submission ID K241414
Product Code DXF
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.5175
Decision Date 2024-09-26
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CrossWise RF Transseptal Access System (Models: CW-1085S, CW-1085A, CW-1012W, CW-1012C); CrossWise RF Adapter Cable (Model CW-1002) received FDA 510(k) clearance under submission number K241414, sponsored by Circa Scientific, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2024-09-26.

Classification & Regulation

This clearance is catalogued under FDA product code DXF and 21 CFR 870.5175, within the Cardiovascular review panel as a Class II device.