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INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S044 · decided 2015-04-01

Approval details

PMA number
P900033
Supplement
S044
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA ARTIFICIAL SKIN DERMAL REGENERATION TEMPLATE
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2015-03-02
Decision date
2015-04-01
Days to decision
30 days
Decision code
OK30
Product code
MDD
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
QUALIFICATION OF THE YOKOGAWA PAPERLESS CHART RECORDING SYSTEM AT THE PLAINSBORO, NEW JERSEY MANUFACTURING LOCATION.

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510(k) clearances by this applicant

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