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INTEGRA(R) DERMAL REGENERATION TEMPLATE, INTEGRA(R) MESHED DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S053 · decided 2016-05-09

Approval details

PMA number
P900033
Supplement
S053
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
INTEGRA(R) DERMAL REGENERATION TEMPLATE, INTEGRA(R) MESHED DERMAL REGENERATION TEMPLATE
Generic name
Device, dermal replacement
Applicant
Integra Lifesciences Corp.
Date received
2015-11-03
Decision date
2016-05-09
Days to decision
188 days
Decision code
APPR
Product code
MDD
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
Approval of two new product sizes (i.e., 4cm x 4cm and 7cm x 7cm) and revised packaging that permits inclusion of a stapler and staples in the Integra Omnigraft Dermal Regeneration Matrix kit. The device, as modified, will be marketed under the trade name Omnigraft Dermal Regeneration Matrix.

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