FOR HEALTHCARE PROFESSIONALS
KeyLift®
The expandable interlaminar fusion platform engineered for the surgeons who already chose the predicate. Two implants. Eight sizes. T1 through S1. One reproducible technique.
FDA-cleared · Posterior non-pedicle supplemental fixation · 18 mm & 20 mm sizing
KeyLift advances interlaminar stabilization with expandable in-situ distraction, lamina load-sharing, and implant options designed for both T1–L5 and L5–S1 anatomy. With two implants, eight sizes, and one reproducible technique, KeyLift™ is built to support the way surgeons already operate.
Large
AND GROWING POPULATION WITH DEGENERATIVE LUMBAR DISEASE
13.1M
ESTIMATED U.S. DIAGNOSED DDD CASES IN 2025
600K
U.S. LSS SURGICAL PROCEDURES PERFORMED ANNUALLY
Sources: Degenerative lumbar spine disease burden per Ravindra V.M. et al., Global Spine Journal 2018; U.S. surgical volume per Amplio Spine press release citing the predicate category, Nov 2023. 1,2
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Indications
Moderate lumbar or lumbo‐sacral stenosis after decompression, with or without Grade I stable spondylolisthesis
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Levels
T1–S1 non-cervical, 1 or 2 contiguous levels
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Materials
Ti-6Al-4V ELI per ASTM F136 · Stainless ASTM F138/A564
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Imaging
Radiopaque · MR safety not established
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Setting
Inpatient or outpatient · ASC-compatible
Five sections, written for spine surgeons, pain physicians, ASC directors, and reimbursement leads. Every clinical claim is sourced. Coding examples are educational only.
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1
Why KeyLift
The category-defining differentiators vs. the predicate device and vs. fusion.
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2
Clinical Foundation
FDA pathway, predicate device, and the Level 1 evidence base behind the category.
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3
Surgeon Testimonials
Voice of the co-inventor, early adopters, and the Amplio leadership team.
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4
Reimbursement
Educational coding context, documentation framework, and payment landscape for procedures KeyLift™ may support.
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5
Surgical Training & Ordering
How surgeons get trained, certified, and ordering both XL and XS sets.
AM01-0069-A