Nitinol-Based Continuous Compression

While static constructs lose force as the graft settles, Pressio’s shape-memory architecture provides the active, continuous compression required to support fusion throughout the healing process.

LIFECYCLE-DRIVEN DESIGN

Procedural Excellence by Design

Pressio optimizes the entire relationship between surgeon, implant, and patient by engineering solutions that deliver precision in the operating room and active, continuous compression throughout the entire biological lifecycle of the fusion.

Biological Fixation

Continuous compressive force across the fusion site maintained throughout the entire healing process—a mechanical advantage static plates cannot replicate.

Procedural Simplicity

A streamlined 3-step technique with no complex screw angles or adjunct hardware, making the surgeon self-sufficient by the third case.

Operative Efficiency

Eliminate the 15–25 minute instrument count and tray management process. Open-and-insert workflow saves 20–30 minutes of total OR time per case.

Clinical Economics

Achieve a 41.19 RVU valuation with a clinically differentiated construct that is marketable to patients and drives practice flow.

Legacy Model vs. Pressio CONTINUUM

See exactly where Pressio eliminates cost and complexity at every step of the surgical workflow.

← Swipe to explore →

Feature
Traditional Model
Pressio CONTINUUM
Net Impact
OR Time
15–25 min instrument count
Open and insert
20–30 min saved per case
Instrument Trays
3–4 multi-tray sets
Single-use sterile kit
100% tray elimination
Sterilization
On-site reprocessing
Pre-sterilized
$300–$600+ saved per case
Rep Logistics
Rep coordination required
Kit ships direct to site
Rep-independent
RVU
Standard ACDF reimbursement
Same RVU, lower cost
Higher margin per case
Inventory
Consignment held at facility
Kit direct, no consignment
Near-zero inventory burden
Available Now — FDA Cleared & Commercially Distributed
CONTINUUM™ ACDF Staple
FDA 510(k) Cleared

CONTINUUM™ ACDF Staple

ACDF NITINOL FIXATION SYSTEM

TIDAL® Cervical Fusion Cages
FDA 510(k) Cleared

TIDAL® Cervical Fusion Cages

Cervical Interbody Fusion Device

TIDAL® Anterior Lumbar Interbody Fusion System
FDA 510(k) Cleared

TIDAL® Anterior Lumbar Interbody Fusion System

FUSION IN THE LUMBAR SPINE (L2-S1)

Cervical Nitinol Plate
In Development

Cervical Nitinol Plate

NITINOL CERVICAL PLATE SYSTEM

Surgical Technique
Lateral Lumbar Interbody Fusion
In Development

Lateral Lumbar Interbody Fusion

LATERAL LUMBAR INTERBODY FUSION

Surgical Technique