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ADAPTA/VERSA/SENSIA/RELIA

FDA premarket approval P980035/S146 · decided 2010-01-13

Approval details

PMA number
P980035
Supplement
S146
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
ADAPTA/VERSA/SENSIA/RELIA
Generic name
Pulse generator, permanent, implantable
Applicant
Medtronic, Inc.
Date received
2009-10-08
Decision date
2010-01-13
Days to decision
97 days
Decision code
APPR
Product code
NVZ
Advisory committee
Cardiovascular
Expedited review
No
Location
Mounds View, MN
Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT MEDTRONIC SWISS MANUFACTURING OPERATIONS IN TOLOCHENAZ, SWITZERLAND TO PERFORM FINAL PACKAGING FOR THE DEVICE.

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