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ProLift Expandable System

by Life Spine, Inc. 3 variants

510(k) K190488

ProLift Expandable System is a Class II device made by Life Spine, Inc., cleared under FDA 510(k) K190488 on 23 Jul 2019, 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 NumberK190488 Date23 Jul 2019ClearedStatusActive

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  • Withdrawn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
MAX
Device class
Class II
Regulation
21 CFR Part 888.3080
Advisory committee
Orthopedic
FDA decision
SESE Substantially Equivalent

Related clearances

cited in the FDA summary

Clearances this device's FDA summary refers to, and clearances whose summaries refer to it: a citation, not a claim of equivalence.

Cites

Cited by

Source: 510k-lineage (choiben314), CC BY 4.0

Other devices from Life Spine, Inc.

  • Arx 13-5550-13

    Class II

  • Arx 13-6540-13

    Class II

  • Arx 13-6550-13

    Class II

  • Arx 13-5545-13

    Class II

See all devices from Life Spine, Inc. →