FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Acid, Hyaluronic, Intraarticular
PMA: P940015
·
Supplement: S038
·
Decision Jan 18, 2017
Classifications
1
FEI Numbers
21
Registration Numbers
21
Basic Information
- Device Name
- Acid, Hyaluronic, Intraarticular
- Trade Name
- SYNVISC
- PMA Number
- P940015
- Supplement Number
- S038
- 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
- January 18, 2017
- Date Received
- December 12, 2016
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Reduction in the testing intervals for routine marketed product surveillance stability studies for Synvisc and Synvisc-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 |