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Lift Vb Spinal System

by Medtronic Sofamor Danek, Inc.

510(k) K010930

Lift Vb Spinal System is a Class II device made by Medtronic Sofamor Danek, Inc., cleared under FDA 510(k) K010930 on 24 Oct 2001, 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

Trust

Unverified

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

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK010930 Date24 Oct 2001ClearedStatusActive

Official records

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
MQP
Device class
Class II
Regulation
21 CFR Part 888.3060
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Devices cleared under K010930

4 devices · FDA GUDID

Devices that FDA's GUDID lists as cleared or approved under this submission number. One submission usually covers a whole product family, so the sizes and models are listed here once.

Devices cleared under K010930
UDI-DISize and differences
VERTE-SPAN® Spinal System 8912010
MEDTRONIC SOFAMOR DANEK, INC.
891201000721902035234 —No longer on the market
VERTE-SPAN® Spinal System 8912200
MEDTRONIC SOFAMOR DANEK, INC.
891220000721902035289 —No longer on the market
VERTE-SPAN® Spinal System 8913105
MEDTRONIC SOFAMOR DANEK, INC.
891310500721902035388 —No longer on the market
VERTE-SPAN® Spinal System 8914000
MEDTRONIC SOFAMOR DANEK, INC.
891400020721902068342 —On the market

Similar devices

Other devices filed under FDA product code MQP (Spinal Vertebral Body Replacement Device).

Other devices from Medtronic Sofamor Danek, Inc.

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