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

Bridge Occlusion Balloon

K Number: K153530 · Decision Feb 5, 2016
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
89
Applicant Total
17
Review Days
58

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Basic Information

Device Name
Bridge Occlusion Balloon
K Number
K153530
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.4450
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Spectranetics, Inc.
Date Received
December 9, 2015
Decision Date
February 5, 2016
Product Code
MJN
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
MJN Catheter, Intravascular Occluding, Temporary

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Other Clearances by Spectranetics, Inc.

K Number Device Name
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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. →