FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Acid, Hyaluronic, Intraarticular
PMA: P080020
·
Supplement: S026
·
Decision Mar 15, 2018
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Acid, Hyaluronic, Intraarticular
- Trade Name
- GEL-ONE
- PMA Number
- P080020
- Supplement Number
- S026
- Device Class
- FDA Class 3
- Product Code
- MOZ
- Generic Name
- Acid, hyaluronic, intraarticular
- Medical Specialty
- Unknown
- Advisory Committee
- Orthopedic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- March 15, 2018
- Date Received
- June 28, 2017
- Supplement Type
- 135 Review Track For 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Approval for a change to the water classification scheme for controls of the quality of the water used to manufacture Gel-One.
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 |