Home › Device types › SAI

Ankle Fusion Cage

FDA product code SAI · Class 2 · Orthopedic

1,629

Registered devices

2

Adverse events

0

Recalls

2

510(k) clearances

Devices with this code

Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.Ossera™ AFX — Restor3d, Inc.Ossera™ AFX Instrumentation — Restor3d, Inc.

Query this across every FDA database — by API.

Linked GUDID · 510(k)/PMA · MAUDE · recalls · establishments. Free tier, no card required.

Get your free API key Read the docs

Sourced from public U.S. FDA data. Informational only — not medical or regulatory advice. Not affiliated with the FDA.