COAPTITE INJECTABLE IMPLANT
FDA premarket approval P040047/S007 · decided 2008-07-24
Approval details
- PMA number
- P040047
- Supplement
- S007
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- COAPTITE INJECTABLE IMPLANT
- Generic name
- AGENT, BULKING, INJECTABLE FOR GASTRO-UROLOGY USE
- Applicant
- Merz North America, Inc.
- Date received
- 2008-06-30
- Decision date
- 2008-07-24
- Days to decision
- 24 days
- Decision code
- OK30
- Product code
- LNM
- Advisory committee
- Gastroenterology, Urology
- Expedited review
- No
- Location
- Franksville, WI
- Statement
- CHANGES IN THE METHOD USED TO MONITOR THE STERILIZATION CYCLE FOR THE COAPTITE® INJECTABLE IMPLANT FOR SOFT TISSUE AUGMENTATION.
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510(k) clearances by this applicant
| Record | Firm | Date |
|---|---|---|
| DESCRIBE PFD Patch (K172689) | Merz North America, Inc. | 2017-11-29 |