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INTEGRA DERMAL REGENERATION TEMPLATE - TERMINALLY STERILIZED (IDRT-TS)

FDA premarket approval P900033/S021 · decided 2012-05-24

Approval details

PMA number
P900033
Supplement
S021
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA DERMAL REGENERATION TEMPLATE - TERMINALLY STERILIZED (IDRT-TS)
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2011-10-13
Decision date
2012-05-24
Days to decision
224 days
Decision code
APPR
Product code
MDD
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
APPROVAL FOR A MANUFACTURING SITE LOCATED AT SYNERGY HEALTH AST, LLC IN DENVER, COLORADO.

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