The following data is part of a premarket notification filed by Skeletal Dynamics, Llc with the FDA for Stablyx Cmc Arthroplasty Implant System.
| Device ID | K180744 |
| 510k Number | K180744 |
| Device Name: | Stablyx CMC Arthroplasty Implant System |
| Classification | Prosthesis, Wrist, Carpal Trapezium |
| Applicant | Skeletal Dynamics, LLC 8905 SW 87 Avenue, Suite 201 Miami, FL 33176 |
| Contact | Ana M. Escagedo |
| Correspondent | Ana M. Escagedo Skeletal Dynamics, LLC 8905 SW 87 Avenue, Suite 201 Miami, FL 33176 |
| Product Code | KYI |
| CFR Regulation Number | 888.3770 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2018-03-22 |
| Decision Date | 2018-04-11 |
| Summary: | summary |