REUNION Sacroiliac Joint Fusion System
FDA 510(k) K232211 · Astura Medical
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
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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| K260477 | CATAMARAN SI Joint Fusion SystemOUR · Traditional | Tenon Medical | 04/08/2026SE |
| K253488 | iFuse INTRA Ti Implant SystemOUR · Traditional | SI-BONE, Inc. | 02/11/2026SE |
| K253611 | Falco Fusion SystemOUR · Traditional | Mcnicoll Surgical, Inc. | 01/29/2026SE |
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| K251365 | OptumSI Implant SystemOUR · Traditional | Si Solutions, LLC | 11/20/2025SE |
| K252322 | SIros-X SystemOUR · Traditional | Genesys Spine | 10/22/2025SE |
| K253094 | iFuse Bedrock Granite Implant SystemOUR · Special | SI-BONE, Inc. | 10/09/2025SE |
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| K252346 | OLYMPIC Posterior Spinal Fixation System; MASADA Modular Spinal Fixation SystemNKB · Traditional | 10/21/2025SE |
| K243259 | MASADA Modular Spinal Fixation SystemNKB · Traditional | 01/07/2025SE |
| K240160 | EGPS Navigated InstrumentsOLO · Traditional | 10/17/2024SE |
| K233359 | DOMINION Expandable Corpectomy SystemMQP · Traditional | 03/08/2024SE |
| K231694 | MASADA Modular Spinal Fixation SystemNKB · Traditional | 11/16/2023SE |
| K223335 | SIRION Lateral Lumbar Interbody SystemMAX · Traditional | 05/09/2023SE |
| K222097 | OLYMPIC Deformity Band SystemOWI · Traditional | 05/04/2023SE |
| K222554 | EL CAPITAN Anterior Lumbar Interbody FusionOVD · Traditional | 01/19/2023SE |
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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.