X-spine Pedicle Screw System
FDA 510(k) K152132 · X-Spine Systems, Inc.
510(k) numberK152132
Submission
- Device name
- X-spine Pedicle Screw System
- Applicant
- X-Spine Systems, Inc.
Miamisburg, OH, US - Received
- July 31, 2015
- Decision date
- September 25, 2015
- 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
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|---|---|---|---|
| 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 |
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| K170119 | Calix Lumbar Spinal Implant SystemMAX · Traditional | 09/29/2017SE |
| K171567 | IRIX-A Lumbar Integrated Fusion SystemOVD · Traditional | 08/28/2017SE |
| K171075 | Calix-C Cervical Interbody SpacerODP · Traditional | 08/01/2017SE |
| K170224 | Spider Cervical Plating SystemKWQ · Traditional | 07/06/2017SE |
| K170530 | Butrex Lumbar Buttress Plating SystemKWQ · Special | 03/22/2017SE |
| K160959 | Xsert Lumbar Expandable Interbody SystemMAX · Traditional | 11/17/2016SE |
| K162944 | Irix-C Cervical Integrated Fusion SystemOVE · Traditional | 11/07/2016SE |
| K160428 | Certex Spinal Fixation SystemNKG · Traditional | 05/05/2016SE |
Questions and answers
When was X-spine Pedicle Screw System cleared by the FDA?
X-spine Pedicle Screw System (K152132) received a 510(k) decision of Substantially Equivalent on September 25, 2015, 56 days after the submission was received.
What is the product code of K152132?
The FDA product code is MNI – Orthosis, Spinal Pedicle Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3070.