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INTEGRA ARTIFICIAL SKIN REGENERATION TEMPLATE

FDA premarket approval P900033/S029 · decided 2013-06-10

Approval details

PMA number
P900033
Supplement
S029
Supplement type
30-Day Notice
Supplement reason
Process Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA ARTIFICIAL SKIN REGENERATION TEMPLATE
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2013-05-15
Decision date
2013-06-10
Days to decision
26 days
Decision code
OK30
Product code
MDD
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
IMPLEMENTATION OF SAMPLING PLAN ANALYZER SOFTWARE.

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