FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Acid, Hyaluronic, Intraarticular
PMA: P180040
·
Supplement: S005
·
Decision Jun 28, 2024
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Acid, Hyaluronic, Intraarticular
- Trade Name
- TRILURON®
- PMA Number
- P180040
- Supplement Number
- S005
- 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
- June 28, 2024
- Date Received
- May 31, 2024
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Change to introduce a new superheated water autoclave for the terminal moist-heat sterilization process of the pre-filled syringes
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 |