Orthopedics

Precision AI Surgical Planning System (PAI-SPS)

Precision AI Pty Ltd

FDA
FDA-cleared AI medical device

Intended to be used to assist in the implantation of a specific shoulder arthroplasty device or a set of specific shoulder arthroplasty devices. Indicated to include guiding alignment, making or establishing cuts, selecting, sizing, attaching, positioning or orienting implant components.

FDA Submission Metadata

Submission number
K233992
Decision date
August 2024
FDA panel
Orthopedic
Product code
QHE
Clinical task (npj)
quantification/feature localization
Data modality (npj)
Images

This entry is sourced from the FDA AI/ML-Enabled Medical Devices list. No editorial review yet — the catalogue may add a deeper review of this device in future.

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Regulatory Approvals

FDA
US FDA 510k

K233992

This entry is on our editorial review queue. Full evaluation — performance metrics, clinical evidence, safety record — lands as our review pipeline graduates each device. The information above is what's been verified to date.