PMA
P150017: CARTIVA SYNTHETIC CARTILAGE IMPLANT
FDA PMA · Prosthesis, metatarsophalangeal joint cartilage replacement implant · Cartiva, Inc.
Key facts
| PMA number | P150017 |
|---|---|
| Trade name | CARTIVA SYNTHETIC CARTILAGE IMPLANT |
| Generic name | Prosthesis, metatarsophalangeal joint cartilage replacement implant |
| Applicant | Cartiva, Inc. |
| Owner/operator | FUSMobile, INC |
| Product code | PNW |
| Approval date | Jul 1, 2016 |
| Docket number | 16M-1916 |
| Notice date | Jul 8, 2016 |
| Establishment registration | 3019585303 |
| FEI number | 3019585303 |
At a glance
- 10–99 Supplements
- Dec 10, 2021 Latest supplement decision
- No Withdrawn
- Yes Summary of safety and effectiveness on file
- 10–99 UDI device identifiers (GUDID)
- None MAUDE adverse event reports
- None Recall events
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA approvals
Premarket approval (PMA) is the FDA's most stringent review pathway, required for most Class III devices that support or sustain life or present a potentially unreasonable risk.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: