FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

Turbo-Power Laser Atherectomy Catheter

K Number: K152181 · Decision Nov 12, 2015
Classifications
1
FEI Numbers
53
Registration Numbers
53
Same Product Code
145
Applicant Total
17
Review Days
100

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Basic Information

Device Name
Turbo-Power Laser Atherectomy Catheter
K Number
K152181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4875
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectranetics, Inc.
Date Received
August 4, 2015
Decision Date
November 12, 2015
Product Code
MCW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
MCW Catheter, Peripheral, Atherectomy

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Other Clearances by Spectranetics, Inc.

K Number Device Name
K223472 TightRail Guardian Motorized Dilator Sheath, 9 French (575-009); TightRail Guardian Motorized Dilator Sheath, 11 French (575-011); TightRail Guardian Motorized Dilator Sheath, 13 French (575-013)
K222837 Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
K212784 TightRail Guardian Motorized Dilator Sheath
DEN210024 CavaClear Laser Sheath
K203540 Bridge Occlusion Balloon
K180694 Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
K172687 Turbo-Power (2.0mm) Laser Atherectomy Catheters, Turbo-Power (2.3mm) Laser Atherectomy Catheters
K170059 Spectranetics Turbo-Elite Laser Atherectomy Catheters
K162561 Turbo-Power (2.0mm) Laser Atherectomy Catheters
K161333 TightRail Sub-C Rotating Dilator Sheath
Search all 17 clearances from Spectranetics, Inc. →