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INTEGRA DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S005 · decided 2001-04-30

Approval details

PMA number
P900033
Supplement
S005
Supplement type
Real-Time Process
Supplement reason
Labeling Change - Indications/instructions/shelf life/tradename
Trade name
INTEGRA DERMAL REGENERATION TEMPLATE
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2001-04-13
Decision date
2001-04-30
Days to decision
17 days
Decision code
APPR
Product code
MDD
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
APPROVAL FOR A CHANGE IN THE TRADE NAME. THE DEVICE WILL BE MARKETED UNDER THE TRADE NAME INTEGRA(R) DERMAL REGENERATION TEMPLATE AND IS INDICATED FOR THE POST EXCISIONAL TREATMENT OF LIFE-THREATENING FULL-THICKNESS OR DEEP PARTIAL-THICKNESS THERMAL INJURY WHERE SUFFICIENT AUTOGRAFT IS NOT AVAILABLE AT THE TIME OF EXCISION OR NOT DESIRABLE DUE TO THE PHYSIOLOGICAL CONDITION OF THE PATIENT.

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