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SPECTRANETICS CROSS-PILOT TURBO ELITE SUPPORT CATHETER

K082559 Class II Traditional
Decision Date
2008-12-11
Sponsor / Applicant
Spectranetics Corp.

Technical Specification

510(k) Submission ID K082559
Product Code DQY
Medical Specialty / Panel Cardiovascular
Regulation Citation 21 CFR 870.1250
Decision Date 2008-12-11
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SPECTRANETICS CROSS-PILOT TURBO ELITE SUPPORT CATHETER received FDA 510(k) clearance under submission number K082559, 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 2008-12-11.

Classification & Regulation

This clearance is catalogued under FDA product code DQY and 21 CFR 870.1250, within the Cardiovascular review panel as a Class II device.