Flex-Thread Distal Fibula lntramedullary Nail System
FDA 510(k) K212030 · Flower Orthopedics Corporation Dba Conventus Flower
510(k) numberK212030
Submission
- Device name
- Flex-Thread Distal Fibula lntramedullary Nail System
- Applicant
- Flower Orthopedics Corporation Dba Conventus Flower
Horsham, PA, US - Received
- June 29, 2021
- Decision date
- July 23, 2021
- Decision
- Substantially Equivalent (SESE)
- Type
- Special 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- HSB – Rod, Fixation, Intramedullary And Accessories
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3020
- Specialty
- Orthopedic
- Implant
- Yes
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| K261481 | Pangea Femur Reconstruction SystemHSB · Traditional | Stryker GmbH | 06/29/2026SE |
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| K253155 | Fule Metallic Lockable Intramedullary Nail SystemsHSB · Traditional | Beijing Fule Science & Technology Development… | 06/17/2026SE |
| K253046 | HERA Interlocking Intramedullary Nailing SystemHSB · Traditional | ZheJiang Decans Medical Devices Co., Ltd. | 06/16/2026SE |
| K260146 | Fitbone® Transport and Lengthening SystemHSB · Traditional | Orthofix Srl | 05/19/2026SE |
| K253991 | Fitbone Trochanteric, FITBONE® Transport and Lengthening System, FITBONE® TAAHSB · Traditional | Orthofix Srl | 05/08/2026SE |
| K261043 | AUTOBAHN Nailing SystemHSB · Special | Globus Medical, Inc. | 04/24/2026SE |
| K252016 | Arthrex Humeral NailsHSB · Traditional | Arthrex, Inc. | 03/20/2026SE |
| K252961 | Fusion FibFix NailHSB · Traditional | Fusion Orthopedics USA, LLC | 03/18/2026SE |
More from Fusion Orthopedics USA, LLC
| 510(k) | Device | Decision |
|---|---|---|
| K222390 | Flex-Thread Ulna Intramedullary Nail SystemHSB · Traditional | 11/21/2022SE |
Questions and answers
When was Flex-Thread Distal Fibula lntramedullary Nail System cleared by the FDA?
Flex-Thread Distal Fibula lntramedullary Nail System (K212030) received a 510(k) decision of Substantially Equivalent on July 23, 2021, 24 days after the submission was received.
What is the product code of K212030?
The FDA product code is HSB – Rod, Fixation, Intramedullary And Accessories, a Class II (moderate risk) device regulated under 21 CFR 888.3020.