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Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD)

FDA premarket approval P810031/S065 · decided 2019-04-29

Approval details

PMA number
P810031
Supplement
S065
Supplement type
Normal 180 Day Track
Supplement reason
Change Design/Components/Specifications/Material
Trade name
Sodium Hyaluronate Ophthalmic Viscoelastic Devices (OVD)
Generic name
AID, SURGICAL, VISCOELASTIC
Applicant
Johnson & Johnson Surgical Vision, Inc.
Date received
2018-12-03
Decision date
2019-04-29
Days to decision
147 days
Decision code
APPR
Product code
LZP
Advisory committee
Ophthalmic
Expedited review
No
Location
Irvine, CA
Statement
Approval for Healon GV® PRO, a modification of the Healon5 PRO OVD with the sodium hyaluronate concentration changed from 23 mg/mL to 18 mg/mL. The device, as modified, will be marketed under the trade name Sodium Hyaluronate Ophthalmic Viscoelastc Device (OVD), Healon GV® PRO and is indicated for use in anterior segment ophthalmic surgical procedures of the human eye. The Healon GV® PRO OVD is designed to create and maintain a deep anterior chamber which facilitates manipulation inside the eye

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