The following data is part of a premarket notification filed by Orthofix, Inc. with the FDA for Contours Vsp Iii Volar Plating System.
Device ID | K101936 |
510k Number | K101936 |
Device Name: | CONTOURS VSP III VOLAR PLATING SYSTEM |
Classification | Plate, Fixation, Bone |
Applicant | ORTHOFIX, INC. 1720 BRAY CENTRAL DR. Mckinney, TX 75069 |
Contact | Mary Biggers, Rac |
Correspondent | Mary Biggers, Rac ORTHOFIX, INC. 1720 BRAY CENTRAL DR. Mckinney, TX 75069 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Special |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2010-07-12 |
Decision Date | 2010-10-20 |
Summary: | summary |