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INTEGRA DERMAL REGENERATION TEMPLATE

FDA premarket approval P900033/S063 · decided 2017-09-08

Approval details

PMA number
P900033
Supplement
S063
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Location Change - Manufacturer/Sterilizer/Packager/Supplier
Trade name
INTEGRA DERMAL REGENERATION TEMPLATE
Generic name
Dressing, wound and burn, interactive
Applicant
Integra Lifesciences Corp.
Date received
2017-06-29
Decision date
2017-09-08
Days to decision
71 days
Decision code
APPR
Product code
MGR
Advisory committee
General, Plastic Surgery
Expedited review
No
Location
Plainsboro, NJ
Statement
Approval for the Steris Applied Sterilization Technologies (AST) Electron Beam (E-Beam) processing facility located at 7225 North Noah Drive, Saxonburg, Pennsylvania, 16056, as an alternate E-Beam Sterilization facility for the Integra Regeneration Template (IDRT) product family.

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510(k) clearances by this applicant

RecordFirmDate
Codman Disposable Perforators (K183581)Integra Lifesciences Corp.2019-01-20
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Codman Certas Plus Electronic Tool Kit (K181902)Integra Lifesciences Corp.2018-10-25
CUSA Excel+ (K150682)Integra Lifesciences Corp.2015-12-18
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INTEGRA LICOX PTO2 MONITOR (K131184)Integra Lifesciences Corp.2013-08-30
JARIT, RUGGLES, R&B REDMOND/ REDMOND, MILTEX, MEISTERHAND - KERRISON RONGEURS (K092227)Integra Lifesciences Corp.2010-02-17