Atlas FDA

DURASEAL EXACT SPINE SEALANT SYSTEM

FDA premarket approval P080013/S006 · decided 2011-05-20

Approval details

PMA number
P080013
Supplement
S006
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
DURASEAL EXACT SPINE SEALANT SYSTEM
Generic name
Sealant, dural
Applicant
Integra LifeSciences Corporation
Date received
2011-03-21
Decision date
2011-05-20
Days to decision
60 days
Decision code
APPR
Product code
NQR
Advisory committee
Neurology
Expedited review
No
Location
Planisboro, NJ
Statement
APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL

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