FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Acid, Hyaluronic, Intraarticular
PMA: P080020
·
Supplement: S022
·
Decision Nov 23, 2016
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Acid, Hyaluronic, Intraarticular
- Trade Name
- GEL-ONE
- PMA Number
- P080020
- Supplement Number
- S022
- Device Class
- FDA Class 3
- Product Code
- MOZ
- Generic Name
- Acid, hyaluronic, intraarticular
- Medical Specialty
- Unknown
- Advisory Committee
- Orthopedic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- November 23, 2016
- Date Received
- November 1, 2016
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Sharing of the current facility and equipment used to manufacture Gel-One for the purpose of manufacturing another product in development.
Classifications
This FDA Pre-Market Approval entry is associated with 1 FDA classification via its product code.
| Product Code | Device Name | Device Class | Medical Specialty |
|---|---|---|---|
| MOZ | Acid, Hyaluronic, Intraarticular | FDA class 3 | Unknown |