FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Aid, Surgical, Viscoelastic
PMA: P810025
·
Supplement: S040
·
Decision Oct 1, 2020
Classifications
1
FEI Numbers
27
Registration Numbers
27
Basic Information
- Device Name
- Aid, Surgical, Viscoelastic
- Trade Name
- Amvisc and Amvisc Plus Ophthalmic Viscosurgical Device (OVD)
- PMA Number
- P810025
- Supplement Number
- S040
- Device Class
- FDA Class 3
- Product Code
- LZP
- Generic Name
- AID, SURGICAL, VISCOELASTIC
- Regulation Number
- 886.4275
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- October 1, 2020
- Date Received
- September 2, 2020
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Removal of an in-process raw material quality control test affecting the sodium hyaluronate (NaHy) raw material for the Amvisc and Amvisc Plus Ophthalmic ViscosurgicalDevices (OVDs) and change the release specification criteria for Amvisc and Amvisc Plus OVDs.
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 |
|---|---|---|---|
| LZP | Aid, Surgical, Viscoelastic | FDA class 3 | Ophthalmic |