Euflexxa (1% Sodium Hyaluronate)
FDA premarket approval P010029/S026 · decided 2018-04-26
Approval details
- PMA number
- P010029
- Supplement
- S026
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Euflexxa (1% Sodium Hyaluronate)
- Generic name
- Acid, hyaluronic, intraarticular
- Applicant
- Ferring Pharmaceuticals, Inc.
- Date received
- 2018-03-29
- Decision date
- 2018-04-26
- Days to decision
- 28 days
- Decision code
- OK30
- Product code
- MOZ
- Advisory committee
- Orthopedic
- Expedited review
- No
- Location
- Parsippany, NJ
- Statement
- Modification to a purification step for a sodium hyaluronate intermediate used to manufacture EUFLEXXA.
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