The following data is part of a premarket notification filed by Vilex, Inc. with the FDA for Vilex/duval/orthex Cannulated Bone Screw Db1 Thread, Model F25-xx-09; Vilex Solid Bone Screws Db1 Thread,model F20-xx-00.
Device ID | K014154 |
510k Number | K014154 |
Device Name: | VILEX/DUVAL/ORTHEX CANNULATED BONE SCREW DB1 THREAD, MODEL F25-XX-09; VILEX SOLID BONE SCREWS DB1 THREAD,MODEL F20-XX-00 |
Classification | Screw, Fixation, Bone |
Applicant | VILEX, INC. 345 OLD CURRY HOLLOW RD. Pittsburgh, PA 15236 |
Contact | Abrahim Lavi |
Correspondent | Abrahim Lavi VILEX, INC. 345 OLD CURRY HOLLOW RD. Pittsburgh, PA 15236 |
Product Code | HWC |
CFR Regulation Number | 888.3040 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2001-12-18 |
Decision Date | 2002-03-18 |