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MEDTRONIC. GEM MODEL 7227CX, GEM III DR MODEL 7275, GEM III VR MODEL 7231 AND GEM III AT MODEL 7276

FDA premarket approval P980050/S003 · decided 2001-05-25

Approval details

PMA number
P980050
Supplement
S003
Supplement type
Normal 180 Day Track
Supplement reason
Express GMP Supplement
Trade name
MEDTRONIC. GEM MODEL 7227CX, GEM III DR MODEL 7275, GEM III VR MODEL 7231 AND GEM III AT MODEL 7276
Generic name
Implantable cardioverter defibrillator (non-CRT)
Applicant
Medtronic, Inc.
Date received
2001-02-05
Decision date
2001-05-25
Days to decision
109 days
Decision code
APPR
Product code
LWS
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR AN ALTERNATE FACILITY FOR THE MANUFACTURING, PACKAGING, AND STERILIZATION OF THE MODEL 7227CX, MODEL 7275, MODEL 7231, AND MODEL 7276 IMPLANTABLE CARDIOVERTER DEFIBRILLATORS LOCATED AT MEDTRONIC S.A., TOLOCHENAZ, SWITZERLAND.

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