Atlas FDA

ELCA Coronary Atherectomy Catheters

FDA premarket approval P910001/S124 · decided 2026-02-06

Approval details

PMA number
P910001
Supplement
S124
Supplement type
135 Review Track For 30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ELCA Coronary Atherectomy Catheters
Generic name
DEVICE, ANGIOPLASTY, LASER, CORONARY
Applicant
Spectranetics Corp.
Date received
2025-06-17
Decision date
2026-02-06
Days to decision
234 days
Decision code
APPR
Product code
LPC
Advisory committee
Cardiovascular
Expedited review
No
Location
Colorado Springs, CO
Statement
the use of alternate components in the adhesive supplied to Philips/Spectranetics for the sterile barrier of the packaging system

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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