DERMAGRAFT (HUMAN FIBROBLAST -DERIVED DERMAL SUBSTITUTE)
FDA premarket approval P000036/S018 · decided 2013-05-21
Approval details
- PMA number
- P000036
- Supplement
- S018
- Supplement type
- 30-Day Notice
- Supplement reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Trade name
- DERMAGRAFT (HUMAN FIBROBLAST -DERIVED DERMAL SUBSTITUTE)
- Generic name
- Dressing, wound and burn, interactive
- Applicant
- Shire Regenerative Medicine
- Date received
- 2013-04-25
- Decision date
- 2013-05-21
- Days to decision
- 26 days
- Decision code
- OK30
- Product code
- MGR
- Advisory committee
- General, Plastic Surgery
- Expedited review
- No
- Location
- San Diego, CA
- Statement
- ADDITION OF A LAMINAR FLOW HOOD, FREEZER REPLACEMENT (SINGLE TO DUAL COMPRESSOR), DISTRIBUTION FREEZER TRANSFER TO WAREHOUSE FOR SAMPLE STORAGE, AND AN ADDITION OF A LIQUID NITROGEN STORAGE FREEZER.
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