510(k) K212030
K212030 is an FDA 510(k) premarket notification submitted by Flower Orthopedics Corporation Dba Conventus Flower for the device "Flex-Thread Distal Fibula lntramedullary Nail System". The FDA issued a decision of Substantially Equivalent on Jul 23, 2021. The device falls under product code HSB (Rod, Fixation, Intramedullary And Accessories), a Class II device regulated under 21 CFR 888.3020. Flower Orthopedics Corporation Dba Conventus Flower has 1 other 510(k) clearance on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- Jul 23, 2021
- Date Received
- Jun 29, 2021
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Rod, Fixation, Intramedullary And Accessories
- Device Class
- Class II
- Regulation Number
- 888.3020
- Review Panel
- OR
- Submission Type
- 510(k)