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 |