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 |