Vanguard Reprocessed External Fixation Devices
FDA 510(k) K053051 · Vanguard Medical Concepts, Inc.
510(k) numberK053051
Submission
- Device name
- Vanguard Reprocessed External Fixation Devices
- Applicant
- Vanguard Medical Concepts, Inc.
Lakeland, FL, US - Received
- October 28, 2005
- Decision date
- December 22, 2005
- 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 |
|---|---|---|
| K051616 | Vanguard Reprocessed External Fixation DevicesKTT · Traditional | 09/06/2005SE |
| K051180 | Vanguard Reprocessed External Fixation DevicesKTT · Traditional | 07/22/2005SE |
| K051043 | Vanguard Reprocessed Diagnostic Electrophysiology CathetersNLH · Traditional | 06/06/2005SE |
| K050763 | Vanguard Reprocessed Diagnostic Electrophysiology CathetersNLH · Traditional | 06/01/2005SE |
| K043198 | Vanguard Reprocessed Arthroscopic WandsNUJ · Traditional | 05/27/2005SE |
| K043253 | Vanguard Reprocessed Dilating Tip and Blunt TrocarsNLM · Traditional | 04/08/2005SE |
| K043594 | Vanguard Reprocessed Bladed Trocar, Non-Bladed Trocar, Trocar AccessoriesNLM · Traditional | 03/31/2005SE |
| K043315 | Vanguard Reprocessed Hand-Activated Ultrasonic ScalpelNLQ · Traditional | 03/22/2005SE |
| K043225 | Vanguard Reprocessed Ultrasonic ScalpelNLQ · Traditional | 03/22/2005SE |
| K040751 | Vanguard Reprocessed Diagnostic Electrophysiology CathetersNLH · Traditional | 03/10/2005SE |
Questions and answers
When was Vanguard Reprocessed External Fixation Devices cleared by the FDA?
Vanguard Reprocessed External Fixation Devices (K053051) received a 510(k) decision of Substantially Equivalent on December 22, 2005, 55 days after the submission was received.
What is the product code of K053051?
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.