RADIESSE INJECTABLE IMPLANT
FDA premarket approval P050052/S010 · decided 2008-07-30
Approval details
- PMA number
- P050052
- Supplement
- S010
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- RADIESSE INJECTABLE IMPLANT
- Generic name
- Implant, dermal, for aesthetic use
- Applicant
- Merz North America, Inc.
- Date received
- 2008-06-30
- Decision date
- 2008-07-30
- Days to decision
- 30 days
- Decision code
- OK30
- Product code
- LMH
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- Franksville, WI
- Statement
- ELIMINATING THE USE OF BIOLOGICAL INDICATORS IN THE SECOND STERILIZATION CYCLE IN A SECOND AUTOCLAVE USED TO STERILIZE THE RADIESSE INJECTABLE IMPLANT.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| DESCRIBE PFD Patch (K172689) | Merz North America, Inc. | 2017-11-29 |