Atlas FDA

RESURE SEALANT

FDA premarket approval P130004/S002 · decided 2016-07-21

Approval details

PMA number
P130004
Supplement
S002
Supplement type
Normal 180 Day Track No User Fee
Supplement reason
Postapproval Study Protocol - OSB
Trade name
RESURE SEALANT
Generic name
Ophthalmic Sealant
Applicant
Ocular Therapeutix, Inc.
Date received
2014-02-07
Decision date
2016-07-21
Days to decision
895 days
Decision code
APPR
Product code
PFZ
Advisory committee
Ophthalmic
Expedited review
No
Location
Bedford, MA
Statement
Approval for the ReSure® Sealant Device Exposure Registry post-approval study protocol.

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510(k) clearances by this applicant

RecordFirmDate
OCULAR FORCE GAUGE (K132917)Ocular Therapeutix, Inc.2013-12-20