# K080611: Mesa Spinal System

- Pathway: 510(k) (Special)
- Applicant: K2m, Inc.
- Decided: Mar 4, 2009 after 365 days
- Product code: MNH (Orthosis, Spondylolisthesis Spinal Fixation)
- Device class: 2
- Regulation: 21 CFR 888.3070
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
67 later devices descend from it; 4 cite it directly.
0 of 68 devices 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) Mesa Spinal System: named in the summary without a submission number
- (no number) Range Spinal System: named in the summary without a submission number
- (no number) Zodiac 4.0 Polyaxial Spinal Fixation System: named in the summary without a submission number
- (no number) Universal Spine System: named in the summary without a submission number
- (no number) Moss Miami Spinal System: named in the summary without a submission number
- (no number) Rogozinski Spinal Rod System: named in the summary without a submission number
- (no number) Synergy Spinal System: named in the summary without a submission number

## Most influential descendants
- K112037: Range Spinal System (Mesa and Denali) (2011), 65 descendants of its own
- K120099: Range Spinal System (Mesa and Denali) (2012), 53 descendants of its own
- K112920: Range Spinal System (Mesa and Denali) (2011), 49 descendants of its own
- K120656: Everest Spinal System (2012), 43 descendants of its own
- K132757: Everest Spinal System (2013), 41 descendants of its own

## Indications for use
Non-cervical spinal fixation devices intended for posterior, non-pedicle fixation for the following indications: degenerative disc disease ( DDD ) (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies ); spondylolisthesis; trauma ( i.e. fracture or dislocation ); spinal stenosis; curvatures ( i.e. scoliosis, kyphosis; and/or lordosis); tumor; pseudoarthrosis; and failed previous fusion. Non-cervical pedicle screw fixation for the following indications: trauma ( i.e. fracture or dislocation); spinal stenosis; curvatures (i.e. scoliosis, kyphosis; and/or lordosis); tumor; pseudoarthrosis; and failed previous fusion. It is also indicated for the treatment of severe spondylolisthesis ( grades 3 and 4 ) of the L5-S I vertebra in skeletally mature patients receiving fusion by autogenous bone graft having implants attached to the lumbar and sacral spine (L3 to sacrum ) with removal of the implants after the attainment of a solid fusion.

Source page: https://510kreport.com/device/K080611
Methodology: https://510kreport.com/methodology