FDA PMA
FDA Class 3
30-Day Notice Accepted
🇺🇸 United States
Ring, Endocapsular
PMA: P030023
·
Supplement: S008
·
Decision Jul 21, 2022
Classifications
1
FEI Numbers
10
Registration Numbers
10
Basic Information
- Device Name
- Ring, Endocapsular
- Trade Name
- RingJect and Capsular Tension Ring (CTR)
- PMA Number
- P030023
- Supplement Number
- S008
- Device Class
- FDA Class 3
- Product Code
- MRJ
- Generic Name
- Ring, endocapsular
- Medical Specialty
- Unknown
- Advisory Committee
- Ophthalmic
- Decision
- 30-Day Notice Accepted
- Decision Code
- OK30
- Decision Date
- July 21, 2022
- Date Received
- February 8, 2022
- Supplement Type
- 30-Day Notice
- Supplement Reason
- Process Change - Manufacturer/Sterilizer/Packager/Supplier
- Expedited Review
- N
Advisory Committee Statement
Change to the processing agent used in the milling process for the Capsular Tension Ring (CTR) and RingJect.
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 |
|---|---|---|---|
| MRJ | Ring, Endocapsular | FDA class 3 | Unknown |