FDA PMA
FDA Class 3
Approved
🇺🇸 United States
Lens, Intraocular, Toric Optics
PMA: P030002
·
Supplement: S034
·
Decision Jun 2, 2015
Classifications
1
FEI Numbers
19
Registration Numbers
19
Basic Information
- Device Name
- Lens, Intraocular, Toric Optics
- Trade Name
- TRULIGN TORIC POSTERIOR CHAMBER INTRAOCULAR LENS
- PMA Number
- P030002
- Supplement Number
- S034
- Device Class
- FDA Class 3
- Product Code
- MJP
- Generic Name
- LENS, INTRAOCULAR, TORIC OPTICS
- Regulation Number
- 886.3600
- Medical Specialty
- Ophthalmic
- Advisory Committee
- Ophthalmic
- Decision
- Approved
- Decision Code
- APPR
- Decision Date
- June 2, 2015
- Date Received
- April 1, 2015
- Supplement Type
- Normal 180 Day Track No User Fee
- Supplement Reason
- Postapproval Study Protocol - OSB
- Expedited Review
- N
Advisory Committee Statement
APPROVAL OF THE POST-APPROVAL STUDY PROTOCOL.
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 |
|---|---|---|---|
| MJP | Lens, Intraocular, Toric Optics | FDA class 3 | Ophthalmic |