Smart Correction System
FDA 510(k) K193368 · Wishbone Medical, Inc.
510(k) numberK193368
Submission
- Device name
- Smart Correction System
- Applicant
- Wishbone Medical, Inc.
Warsaw, IN, US - Received
- December 5, 2019
- Decision date
- September 18, 2020
- 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 |
|---|---|---|
| K231461 | Smart Correction System (HA Half Pins)KTT · Special | 06/16/2023SE |
| K230527 | WishBone Medical Plate and Screw SystemHRS · Special | 03/29/2023SE |
| K221366 | Smart Correction System Rings and Compatible HA-Coated Half PinsKTT · Special | 06/06/2022SE |
| K213489 | Wishbone Medical Plate and Screw System: 3.0mm Screws and 7-Hole Straight Fibula PlateHRS · Traditional | 01/27/2022SE |
| K203467 | WishBone Medical Plate and Screw SystemHWC · Special | 12/23/2020SE |
| K182704 | WishBone Guided Growth SystemOBT · Traditional | 06/25/2019SE |
| K180736 | WishBone Medical Plate and Screw SystemHRS · Traditional | 10/04/2018SE |
| K173013 | WishBone K-Wire SystemHTY · Traditional | 12/14/2017SE |
Questions and answers
When was Smart Correction System cleared by the FDA?
Smart Correction System (K193368) received a 510(k) decision of Substantially Equivalent on September 18, 2020, 288 days after the submission was received.
What is the product code of K193368?
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.