The following data is part of a premarket notification filed by Smith & Nephew, Inc. with the FDA for Vlp Foot Talus Plates, Vlp Percutaneous Calcaneus Plates And Misc Vlp Bone Screws, Peri-loc Ankle Fusion Plates.
Device ID | K110670 |
510k Number | K110670 |
Device Name: | VLP FOOT TALUS PLATES, VLP PERCUTANEOUS CALCANEUS PLATES AND MISC VLP BONE SCREWS, PERI-LOC ANKLE FUSION PLATES |
Classification | Plate, Fixation, Bone |
Applicant | SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Contact | David Henley |
Correspondent | David Henley SMITH & NEPHEW, INC. 1450 BROOKS RD. Memphis, TN 38116 |
Product Code | HRS |
CFR Regulation Number | 888.3030 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2011-03-09 |
Decision Date | 2011-07-12 |
Summary: | summary |