Restylane Refyne, Restylane Defyne Injectable Gels
FDA premarket approval P140029/S006 · decided 2018-05-11
Approval details
- PMA number
- P140029
- Supplement
- S006
- Supplement type
- 135 Review Track For 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- Restylane Refyne, Restylane Defyne Injectable Gels
- Generic name
- Implant, dermal, for aesthetic use
- Applicant
- Q-Med AB
- Date received
- 2017-12-18
- Decision date
- 2018-05-11
- Days to decision
- 144 days
- Decision code
- APPR
- Product code
- LMH
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Uppsala
- Statement
- Approval for a replacement of a compressor for compressed air used in the manufacture of Restylane Refyne and Restylane Defyne.
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