Lower Extremity External Fixation - Expanded Indications
FDA 510(k) K081244 · Biomet Trauma
510(k) numberK081244
Submission
- Device name
- Lower Extremity External Fixation - Expanded Indications
- Applicant
- Biomet Trauma
Warsaw, IN, US - Received
- May 1, 2008
- Decision date
- July 30, 2008
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3030
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code KTT
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K254087 | MAXFRAME AUTOSTRUT with Bluetooth Multi-Axial Correction SystemKTT · Traditional | Synthes (USA) Products, LLC | 06/11/2026SE |
| K260900 | DYNEX® External Fixation SystemsKTT · Special | Vilex, LLC | 04/17/2026SE |
| K260112 | QuikFix External Fixator: Knee-Spanning PackKTT · Traditional | Stabiliz Orthopaedics, Inc. | 03/23/2026SE |
| K253291 | Excelsior SystemKTT · Traditional | Blue Ocean Global | 01/20/2026SE |
| K253613 | Monkey Rings External Ring Fixation SystemKTT · Special | Paragon 28, Inc. | 12/19/2025SE |
| K253202 | Hoffmann LRF SystemKTT · Traditional | Stryker GmbH | 12/19/2025SE |
| K252555 | Medusa Orthopedics Boa External Fixation SystemKTT · Traditional | Medusa Orthopedics, LLC | 11/25/2025SE |
| K252625 | The Response Ortho Smart Fixator - Hexapod SystemKTT · Traditional | Response Ortho Solutions, LLC | 11/20/2025SE |
| K252106 | External Fixation Mini Rail SystemKTT · Traditional | Paragon 28, Inc. | 09/30/2025SE |
| K251862 | External Fixation Bone DistractorKTT · Traditional | Paragon 28, Inc. | 08/11/2025SE |
More from Paragon 28, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K091976 | Biomet Phoenix Ankle Nail and Ankle Arthrodesis NailHSB · Traditional | 08/17/2009SE |
| K092078 | Optilock Periarticular PlatingHRS · Special | 08/05/2009SE |
| K082874 | Biodrive Cannulated Screw SystemHWC · Traditional | 02/05/2009SE |
| K081243 | Biomet Phoenix Ankle Nail SystemHSB · Traditional | 06/27/2008SE |
| K071325 | Biomet Variable Locking Plate SystemHRS · Traditional | 07/26/2007SE |
| K070823 | Growth Control Plating SystemHRS · Traditional | 05/07/2007SE |
Questions and answers
When was Lower Extremity External Fixation - Expanded Indications cleared by the FDA?
Lower Extremity External Fixation - Expanded Indications (K081244) received a 510(k) decision of Substantially Equivalent on July 30, 2008, 90 days after the submission was received.
What is the product code of K081244?
The FDA product code is KTT – Appliance, Fixation, Nail/Blade/Plate Combination, Multiple Component, a Class II (moderate risk) device regulated under 21 CFR 888.3030.