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2.5MM TURBO ELITE 035, 2.3MM TURBO ELITE 035

K123632 Class II Traditional
Decision Date
2013-01-25
Sponsor / Applicant
Spectranetics Corp.

Technical Specification

510(k) Submission ID K123632
Product Code MCW
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.4875
Decision Date 2013-01-25
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

2.5MM TURBO ELITE 035, 2.3MM TURBO ELITE 035 received FDA 510(k) clearance under submission number K123632, sponsored by Spectranetics Corp.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Cardiovascular review panel. The statutory decision date of record is 2013-01-25.

Classification & Regulation

This clearance is catalogued under FDA product code MCW and 21 CFR 870.4875, within the Cardiovascular review panel as a Class II device.