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INTEGRA DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S015 · decided 2007-02-09

Approval details

PMA number
P900033
Supplement
S015
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA DERMAL REGENERATION TEMPLATE
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2007-01-12
Decision date
2007-02-09
Days to decision
28 days
Decision code
OK30
Product code
MDD
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
ALTERNATE ALKALI TREATMENT PRODUCTION AREA.

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