Cd Horizon Spinal System

by Medtronic Sofamor Danek, Inc. 29 variants

510(k) K102807

Cd Horizon Spinal System is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K102807 on 17 Nov 2010, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

510(k) K102807↗

FDA record

Trust

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

Region	Authorization	Number	Date	Status
United States	FDA 510(k)SESU Special	NumberK102807	Date17 Nov 2010Cleared	StatusActive

Official records

FDA 510(k) database 510(k) number K102807

Coverage

1 jurisdiction

Active
Expiring
Withdrawn
Listed
Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number: K102807
FDA product code: NKB

Device class: Class II
Regulation: 21 CFR Part 888.3070
Advisory committee: Orthopedic
FDA decision: SESU

Other devices from Medtronic Sofamor Danek, Inc.

MSB Reusable Instruments 9870005

Class I
MSB CD HORIZON Spinal System 6530530

Class II
T2 STRATOSPHERE™ Expandable Corpectomy System 436125C

Class II
MSB SHILLA Growth Guidance System 7670431

Class II

See all devices from Medtronic Sofamor Danek, Inc. →