Atlas FDA

VCFix Spinal System

FDA 510(k) clearance K250637 · decided 2025-05-30

Clearance details

K-number
K250637
Device name
VCFix Spinal System
Applicant
Amber Implants
Decision
Substantially Equivalent
Date received
2025-03-03
Decision date
2025-05-30
Days to decision
88 days
Clearance type
Traditional
Product code
NDN
Device class
2
Regulation number
888.3027
Medical specialty
Orthopedic
Advisory committee
Orthopedic
Location
The Hague, NL
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
XeliteMed SuperM-Fix Spinal Bone Cement (K251896)Xelite Biomed , Ltd.2026-01-28
XeliteMed VertehighFix High Viscosity Spinal Bone Cement System (K243537)Xelite Biomed , Ltd.2025-04-11
XeliteMed VertehighFix High Viscosity Spinal Bone Cement (K241775)Xelite Biomed , Ltd.2024-09-18
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Renova Spine Balloon Catheter (K231340)Biopsybell S.R.L.2023-10-30
INJECTION PIN (KIP(02031-02061) (03031-03061)) (K221697)Slk Ortho, LLC2023-03-03
SpineJack® Expansion Kit (K223294)Stryker Instruments2022-12-20
KYPHON VuE Bone Cement (K220131)Tecres S.P.A.2022-04-18
TRACKER Plus Kyphoplasty System (K211797)GS Medical Co., Ltd.2021-10-28
SpineJack Expansion Kit, Vertaplex Radiopaque Bone Cement, Vertaplex HV Radiopaque Bone Cement (K211238)Stryker Instruments2021-06-25
SpineJack Expansion Kit (K202393)Stryker Corporation2020-10-20

Recalls involving this device

No recalls on record reference this clearance.