REUNION Sacroiliac Joint Fusion System

FDA 510(k) K232211 · Astura Medical

Substantially Equivalent

510(k) numberK232211

Submission

Device name
REUNION Sacroiliac Joint Fusion System
Applicant
Astura Medical
Irving, TX, US
Received
July 26, 2023
Decision date
October 24, 2023
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
OUR – Sacroiliac Joint Fixation
Device class
Class II (moderate risk)
Regulation
21 CFR 888.3040
Specialty
Orthopedic
Implant
Yes

sacroiliac joint fusion

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Questions and answers

When was REUNION Sacroiliac Joint Fusion System cleared by the FDA?

REUNION Sacroiliac Joint Fusion System (K232211) received a 510(k) decision of Substantially Equivalent on October 24, 2023, 90 days after the submission was received.

What is the product code of K232211?

The FDA product code is OUR – Sacroiliac Joint Fixation, a Class II (moderate risk) device regulated under 21 CFR 888.3040.