SCULPTRA®
FDA premarket approval P030050/S049 · decided 2024-03-07
Approval details
- PMA number
- P030050
- Supplement
- S049
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- SCULPTRA®
- Generic name
- Implant, dermal, for aesthetic use
- Applicant
- Q-Med AB
- Date received
- 2024-02-09
- Decision date
- 2024-03-07
- Days to decision
- 27 days
- Decision code
- OK30
- Product code
- LMH
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Uppsala
- Statement
- Implementation of automatic visual inspection equipment in the manufacture of the Sculptra products.
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