The following data is part of a premarket notification filed by Skeletal Dynamics, Llc with the FDA for Align Radial Head System.
| Device ID | K092721 |
| 510k Number | K092721 |
| Device Name: | ALIGN RADIAL HEAD SYSTEM |
| Classification | Prosthesis, Elbow, Hemi-, Radial, Polymer |
| Applicant | SKELETAL DYNAMICS, LLC 80 SHELDON TECHNOLOGY CENTER Shelton, CT 06484 |
| Contact | Joseph Azary |
| Correspondent | Joseph Azary SKELETAL DYNAMICS, LLC 80 SHELDON TECHNOLOGY CENTER Shelton, CT 06484 |
| Product Code | KWI |
| CFR Regulation Number | 888.3170 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2009-09-04 |
| Decision Date | 2010-08-03 |
| Summary: | summary |