← FDA Medical Device Classifications
Aortic Annuloplasty Ring
PST · Class II — Moderate Risk (510(k) clearance required) · Cardiovascular · 21 CFR 870.3800
Classification
- FDA Product Code
PST- Device class
- Class II — Moderate Risk (510(k) clearance required)
- Regulation
- 21 CFR 870.3800
- Review panel
- CV
- Medical specialty
- Cardiovascular
- Submission type
- 1
- GMP exempt
- N
- Life sustaining
- Y
- Implant
- Y
- Third-party review
- N
Definition
To correct annular dilatation and/or maintain annular geometry of the aortic valve.
Market data
- Cleared 510(k) submissions
- 2
- Registered establishments
- 4
Source
- Authoritative
- FDA Device Classification database
- Machine
- JSON-LD · Markdown