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INTEGRA ARTIFICIAL SKIN, DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S020 · decided 2012-05-04

Approval details

PMA number
P900033
Supplement
S020
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA ARTIFICIAL SKIN, DERMAL REGENERATION TEMPLATE
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2011-08-01
Decision date
2012-05-04
Days to decision
277 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 INTEGRA NEUROSCIENCES IN ANASCO, PUERTO RICO.

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510(k) clearances by this applicant

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