RESTYLANE INJECTABLE GEL
FDA premarket approval P040024/S009 · decided 2007-06-05
Approval details
- PMA number
- P040024
- Supplement
- S009
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- RESTYLANE INJECTABLE GEL
- Generic name
- Implant, dermal, for aesthetic use
- Applicant
- Q-Med AB
- Date received
- 2007-05-11
- Decision date
- 2007-06-05
- Days to decision
- 25 days
- Decision code
- OK30
- Product code
- LMH
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Uppsala
- Statement
- NEW WATER SYSTEM AND A NEW SYSTEM FOR MANAGING MATERIALS AT THE Q-MED MANUFACTURING FACILITY.
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