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INTEGRA ARTIFICAL SKIN DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S056 · decided 2016-09-15

Approval details

PMA number
P900033
Supplement
S056
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA ARTIFICAL SKIN DERMAL REGENERATION TEMPLATE
Generic name
Dressing, wound and burn, interactive
Applicant
Integra Lifesciences Corp.
Date received
2016-08-19
Decision date
2016-09-15
Days to decision
27 days
Decision code
OK30
Product code
MGR
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
Replacement of a portion of the water deionization (DI) system, located in the Collagen Manufacturing Center. Integra will replace a portion of the DI system with a new Evoqua IonRight GEN3 system. The change is being made to lower operating expenses, as well as reduce the frequency of service of the system by reducing the frequency at which the vessels are shipped off site for regeneration.

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