PMA supplement
P150017 S003: CARTIVA SYNTHETIC CARTILAGE IMPLANT
FDA PMA supplement · Real-Time Process · Cartiva, Inc.
Key facts
| Original PMA | P150017 |
|---|---|
| Supplement number | S003 |
| Supplement type | Real-Time Process |
| Reason for the supplement | Process Change - Manufacturer/Sterilizer/Packager/Supplier |
| Trade name | CARTIVA SYNTHETIC CARTILAGE IMPLANT |
| Generic name | Prosthesis, metatarsophalangeal joint cartilage replacement implant |
| Applicant | Cartiva, Inc. |
| Product code | PNW |
| Received date | Aug 15, 2016 |
| Decision date | Nov 1, 2016 |
At a glance
- No Expedited review granted
- No Approval order on file
- No Summary of safety and effectiveness on file
Counts are shown as ranges. Exact figures, trends and every underlying record are available in Orca1.
About PMA supplements
A PMA supplement asks FDA to approve a change to a device that already holds a premarket approval: a new indication, a design or labeling change, a manufacturing site or process change.
Source: U.S. Food and Drug Administration (FDA), Premarket Approval (PMA) database · Source date: