The following data is part of a premarket notification filed by Conventus Orthopaedics, Llc with the FDA for Flex-threadtm Distal Fibula Intramedullary Nail System.
Device ID | K202858 |
510k Number | K202858 |
Device Name: | Flex-ThreadTM Distal Fibula Intramedullary Nail System |
Classification | Rod, Fixation, Intramedullary And Accessories |
Applicant | Conventus Orthopaedics, LLC 10200 73rd Ave N. Suite 122 Maple Grove, MN 55369 |
Contact | Amanda Pentecost |
Correspondent | Amanda Pentecost Conventus Orthopaedics, LLC 10200 73rd Ave N. Suite 122 Maple Grove, MN 55369 |
Product Code | HSB |
CFR Regulation Number | 888.3020 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 2020-09-28 |
Decision Date | 2021-01-22 |