True Spinal Fixation System
FDA 510(k) K130958 · Innovative Surgical Designs
510(k) numberK130958
Submission
- Device name
- True Spinal Fixation System
- Applicant
- Innovative Surgical Designs
Bloomington, IN, US - Received
- April 5, 2013
- Decision date
- October 17, 2013
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
- Summary
- 510(k) summary available from FDA
Device classification
- Product code
- MNI – Orthosis, Spinal Pedicle Fixation
- Device class
- Class II (moderate risk)
- Regulation
- 21 CFR 888.3070
- Specialty
- Orthopedic
- Implant
- Yes
Other 510(k)s with product code MNI
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K171497 | Mikron Spinal Fixation SystemMNI · Traditional | Mikron Makina Sanayi Ticaret Co. , Ltd. | 10/12/2017SE |
| K160731 | LumFix Spinal Fixation SytemMNI · Traditional | CG Bio Co., Ltd. | 10/04/2016SE |
| K151458 | Double Medical Universal Spine SystemMNI · Traditional | Double Medical Technology, Inc. | 08/22/2016SE |
| K153273 | MySpine Pedicle Screw Placement Guides - LPMNI · Traditional | Medacta International S.A. | 06/29/2016SE |
| K160124 | LUMIS Cannulated Pedicle Screw Fixation System, U.L.I.S. Pedicle Screw Fixation SystemMNI · Special | Spinevision S.A. | 04/04/2016SE |
| K160320 | PremierMNI · Traditional | Shandong Weigao Orthopaedic Device Co., Ltd. | 04/01/2016SE |
| K160003 | Sniper (R) Spine SystemMNI · Traditional | Spine Wave, Inc. | 02/26/2016SE |
| K152324 | YAHUA Spinal SystemMNI · Traditional | Beijing Weigao Yahua Artificial Joint… | 02/01/2016SE |
| K143222 | FIREFLY Pedicle Screw Navigation GuideMNI · Traditional | Mighty Oak Medical, Inc. | 12/11/2015SE |
| K150684 | WASTON General Spinal SystemMNI · Traditional | Changzhou Waston Medical Appliance Co., Ltd. | 11/18/2015SE |
More from Changzhou Waston Medical Appliance Co., Ltd.
| 510(k) | Device | Decision |
|---|---|---|
| K220297 | True Tulip, True M.I.S.NKB · Traditional | 09/16/2022SE |
| K212627 | True Tulip, True M.I.S.NKB · Special | 02/18/2022SE |
| K210816 | True Tulip, True M.I.S.NKB · Special | 05/18/2021SE |
| K201780 | True Tulip System, True M.I.S. SystemNKB · Special | 07/22/2020SE |
| K181584 | Redi-SpineNKB · Traditional | 08/10/2018SE |
| K171559 | True Spinal Fixation SystemNKB · Traditional | 07/24/2017SE |
| K170710 | True Spinal Fixation SystemNKB · Traditional | 07/14/2017SE |
| K133690 | True Spinal Fussion SystemMNH · Traditional | 05/07/2014SE |
Questions and answers
When was True Spinal Fixation System cleared by the FDA?
True Spinal Fixation System (K130958) received a 510(k) decision of Substantially Equivalent on October 17, 2013, 195 days after the submission was received.
What is the product code of K130958?
The FDA product code is MNI – Orthosis, Spinal Pedicle Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3070.