FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Ophthalmic Sealant
PMA: P130004
·
Supplement: S008
·
Decision May 5, 2020
Classifications
1
FEI Numbers
2
Registration Numbers
2
Basic Information
- Device Name
- Ophthalmic Sealant
- Trade Name
- ReSure Sealant
- PMA Number
- P130004
- Supplement Number
- S008
- Device Class
- FDA Class 3
- Product Code
- PFZ
- Generic Name
- Ophthalmic Sealant
- Medical Specialty
- Unknown
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- May 5, 2020
- Date Received
- December 11, 2019
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol
- Expedited Review
- N
Advisory Committee Statement
Approval of the revised protocol for the post-approval study (PAS), Device Exposure Registry Study.
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 |
|---|---|---|---|
| PFZ | Ophthalmic Sealant | FDA class 3 | Unknown |