Atlas FDA

CORDIS AVANTI+CATHETER SHEATH INTRODUCER SYSTEM

FDA 510(k) clearance K970392 · decided 1997-04-24

Clearance details

K-number
K970392
Device name
CORDIS AVANTI+CATHETER SHEATH INTRODUCER SYSTEM
Applicant
Cordis Corp.
Decision
Substantially Equivalent
Date received
1997-02-03
Decision date
1997-04-24
Days to decision
80 days
Clearance type
Traditional
Product code
DRE
Device class
2
Regulation number
870.1310
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Miami Lakes, FL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

RecordFirmDate
CORDIS AVANTI + CATHETER SHEATH INTRODUCER SYSTEM The product includes a Catheter Sheath I recall (Z-1174-2016)Cordis Corporation2016-03-15

PMA approvals by this applicant

RecordFirmDate
CYPHER SIROLIMUS-ELUTING CORONARY STENT (P020026/S086)Cordis Corp.2014-10-10
CYPHER SIROLIMUS-ELUTING CORONARY STENT (P020026/S082)Cordis Corp.2012-01-27
CYPHER SIROLIMUS-ELUTING CORONARY STENT (P020026/S085)Cordis Corp.2012-01-26
CYPHER SIROLIMUS-ELUTING CORONARY STENT ON RAPTOR OVER-THE-WIRE DELIVERY SYSTEM/RAPTORRAIL RAPID EXCHANGE DELIVERY SYSTE (P020026/S059)Cordis Corp.2011-05-27
CYPHER SIROLIMUS CORONARY STENT ON RAPTOR OTW DELIVERY SYSTEM OR RAPTORRAIL RAPID EXCHANGE DELIVERY SYSTEM (CYPHER STENT (P020026/S083)Cordis Corp.2011-05-27
CYPHER SIROLIMUS-ELUTING CORONARY STENT ON RAPTOR OTW DELIVERY SYSTEM/RAPTORRAIL RAPID EXCHANGE DELIVERY SYSTEM (CYPHER (P020026/S081)Cordis Corp.2011-03-03
CYPHER SIROLIMUS -ELUTING CORONARY STENT (4.0 MM) (P020026/S026)Cordis Corp.2011-02-22
CYPHER SIROLIMUS-ELUTING CORONARY STENT ON RAPTOR OTW DELIVERY SYSTEM/RAPTORRAIL RAPID EXCHANGE DELIVERY SYSTEM (P020026/S078)Cordis Corp.2010-09-02