VCFix Spinal System

FDA 510(k) K250637 · Amber Implants

Substantially Equivalent

510(k) numberK250637

Submission

Device name
VCFix Spinal System
Applicant
Amber Implants
The Hague, NL
Received
March 3, 2025
Decision date
May 30, 2025
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
NDN – Cement, Bone, Vertebroplasty
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3027
Specialty
Orthopedic
Implant
Yes

Other 510(k)s with product code NDN

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K251896XeliteMed SuperM-Fix Spinal Bone CementNDN · Traditional Xelite Biomed , Ltd.01/28/2026SE
K243537XeliteMed VertehighFix High Viscosity Spinal Bone Cement SystemNDN · Traditional Xelite Biomed , Ltd.04/11/2025SE
K241775XeliteMed VertehighFix High Viscosity Spinal Bone CementNDN · Traditional Xelite Biomed , Ltd.09/18/2024SE
K232842Balloon Inflation SystemNDN · Traditional Ningbo Hicren Biotechnology Co., Ltd.02/29/2024SE
K240084V-STRUT® Vertebral ImplantNDN · Special Hyprevention02/09/2024SE
K231340Renova Spine Balloon CatheterNDN · Traditional Biopsybell S.R.L.10/30/2023SE
K221697Injection Pin (KIP(02031-02061) (03031-03061))NDN · Traditional Slk Ortho, LLC03/03/2023SE
K223294SpineJack® Expansion KitNDN · Traditional Stryker Instruments12/20/2022SE
K220131KYPHON VuE Bone CementNDN · Traditional Tecres S.P.A.04/18/2022SE
K211797TRACKER Plus Kyphoplasty SystemNDN · Traditional GS Medical Co., Ltd.10/28/2021SE

Questions and answers

When was VCFix Spinal System cleared by the FDA?

VCFix Spinal System (K250637) received a 510(k) decision of Substantially Equivalent on May 30, 2025, 88 days after the submission was received.

What is the product code of K250637?

The FDA product code is NDN – Cement, Bone, Vertebroplasty, a Class II (moderate risk) device regulated under 21 CFR 888.3027.