FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Acid, Hyaluronic, Intraarticular
PMA: P980044
·
Supplement: S006
·
Decision Mar 7, 2007
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Acid, Hyaluronic, Intraarticular
- Trade Name
- SUPARTZ
- PMA Number
- P980044
- Supplement Number
- S006
- 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 7, 2007
- Date Received
- January 30, 2007
- Supplement Type
- Special (Immediate Track)
- Supplement Reason
- Labeling Change - Indications/instructions/shelf life/tradename
- Expedited Review
- N
Advisory Committee Statement
APPROVAL FOR ADDING BOTH POSSIBLE ADVERSE REACTIONS REPORTED WORLDWIDE TO THE INSTRUCTION FOR USE, AND THE POSSIBLE SIDE EFFECTS COLLECTED FROM WORLDWIDE POST-MARKET EXPERIENCE TO THE PATIENT INFORMATION BROCHURE.
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 |