Atlas FDA

ELCA Coronoary Laser Atherectomy Catheter

FDA premarket approval P910001/S116 · decided 2022-08-19

Approval details

PMA number
P910001
Supplement
S116
Supplement type
Real-Time Process
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ELCA Coronoary Laser Atherectomy Catheter
Generic name
DEVICE, ANGIOPLASTY, LASER, CORONARY
Applicant
Spectranetics Corp.
Date received
2022-06-17
Decision date
2022-08-19
Days to decision
63 days
Decision code
APPR
Product code
LPC
Advisory committee
Cardiovascular
Expedited review
No
Location
Colorado Springs, CO
Statement
Approval for implementing new catheter bonding materials.

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510(k) clearances by this applicant

RecordFirmDate
LEXICONTURE MECHANICAL DILATOR SHEATH SET (K140047)Spectranetics Corp.2014-04-09
2.5MM TURBO ELITE 035, 2.3MM TURBO ELITE 035 (K123632)Spectranetics Corp.2013-01-25
8FR TURBO - TANDEM SYSTEM (K112032)Spectranetics Corp.2011-10-17
TORQMAX SHEATH GRIP ACCESSORY (K093257)Spectranetics Corp.2010-03-26
TURBO-TANDEM SYSTEM MODEL 472-110 (K094036)Spectranetics Corp.2010-01-25
SPECTRANETICS VISISHEATH DILATOR SHEATH (K092378)Spectranetics Corp.2009-11-02
SPECTRANETICS QUICK CROSS EXTREME SUPPORT CATHETERS (K092396)Spectranetics Corp.2009-09-04
SPECTRANETICS TURBO-TANDEM SYSTEM (K091299)Spectranetics Corp.2009-07-01