# K992885: Versalok Low Back Fixation System

- Pathway: 510(k) (Traditional)
- Applicant: Osteotech, Inc.
- Decided: Nov 19, 1999 after 84 days
- Product code: KWP (Appliance, Fixation, Spinal Interlaminal)
- Device class: 2
- Regulation: 21 CFR 888.3050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Versalok: named in the summary without a submission number
- (no number) SSCS: named in the summary without a submission number
- (no number) ISOLA Spinal System: named in the summary without a submission number

## Indications for use
The VERSALOK Low Back Fixatton System is intended to provide temporary maintenance and support of the correction during the time normally needed for the fusion mass to mature. 1) A construct with screws attached to the pedicles of the lumbar and sacral spine (L3 to S1) and autogenous bone graft may be used only for the treatment of severe spondylolisthesis (grade 3 or 4) at the fifth lumbar — first sacral (L5-S1) vertebral joint (see warning below). The device is intended to be implanted using a posterior surgical approach and removed after the development of a solid fusion mass. 2) When not used as a pedicle screw fixation system, various combinations of the VERSALOK components are also indicated to provide temporary stability of the thoracic, thoracolumbar, or lumbar spine (T1 to S1) during bony fusion healing secondary to: a) Unstable spinal fractures (such as fracture dislocations) or instability secondary to spinal tumors; b) Degenerative disk diseases of the spine (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); c) Spinal curvatures (such as idiopathic scoliosis, neuromuscular scoliosis/kyphoscoliosis with associated paralysis or spasticity, and secondary to spinal fractures) which are: ¢ Progressive, despite other forms of treatment, e Detrimental to cardiopulmonary function, ¢ Interfering with spinal mechanics or causing severe back pain, or e Cosmetically unacceptable, progressive, and painful. For the above indications, use of spinal fixation instrumentation in children has been reported.'? Children should have adequate bony and soft tissue maturity to undergo implantation but need not have reached skeletal maturity. 3) The VERSALOK Low Back Fixation System is also a pedicle screw system intended to provide immobilization and stabilization of spinal segments in skeletally mature patients as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine: degenerative spondylolisthesis with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumor, and failed previous fusion (pseudarthrosis).

Source page: https://510kreport.com/device/K992885
Methodology: https://510kreport.com/methodology