510(k) · Cleared
ClearedCentrion 500 C-Arm System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Osteosys Co.,Ltd · JAA System, X-Ray, Fluoroscopic, Image-Intensified
Cleared on Apr 27, 2005 as substantially equivalent to K003837 (Ge Oec Medical Systems, 2001) after a 22-day review. Its family tree reaches back 1 generation to 2001. 1 of the 2 devices in its family, counting itself, has a Class I recall.
- Decided
- Apr 27, 2005
- Review
- 22 days
- Class
- Class II
- Product code
- JAA
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K003837 (2001). No later device cites it as a predicate yet. 1 of the 2 devices in this family, counting this one, has a Class I recall.
- Root · 1 generation backK003837 Flexiview 8800 Digital Mobile Imaging SystemGe Oec Medical Systems · 2001 · Recalled (Class I)
- This deviceK050866 Centrion 500 C-Arm SystemOsteosys Co.,Ltd · 2005
Class I recalls in this family
- K003837 Flexiview 8800 Digital Mobile Imaging Systemdirect predicate · 2001
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K003837 | Flexiview 8800 Digital Mobile Imaging System | Ge Oec Medical Systems | 2001 | Class I |
| 0 (this device) | K050866 | Centrion 500 C-Arm System | Osteosys Co.,Ltd | 2005 | — |
Sources: FDA 510(k) database (decision fields), the FDA summary (predicates and indications), FDA recall and enforcement reports, and MAUDE; processed by 510(k) Report. Verify on FDA.gov · Methodology and accuracy.
1 device in this family has a Class I recall. A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
Top candidate predicates for a new JAA device
- #1 K253103 Nexus DRF Digital X-ray Imaging Systemscore 13.2 · 7 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (1)
Devices the submitter claimed this one is substantially equivalent to (*), and reference devices cited for a specific test or feature (†), as written in the FDA summary.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K003837 | Flexiview 8800 Digital Mobile Imaging SystemSummary page 1…MARKETED PREDICATE DEVICE The Centrion 500 C-Arm System is substantially equivalent to the General Electric OEC FLEXIVIEW 8800 Digital Mobile Imaging System (K003837). B. DEVICE DESCRIPTION The Centrion 500 C-Arm System. Is a digital C-Arm-type fluoroscopic system. It includes near… | 2001 |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (1 Class I)
No FDA recall names this device.
Relatives with a Class I recall
Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.
- K003837Flexiview 8800 Digital Mobile Imaging SystemGe Oec Medical Systems · 2001 · Direct predicate · ◆ on the line of descent in FIG. 11 Class I recall
What does this lineage say?
- Its one ancestor has a recall, Class I.
- 2 other devices also cite its predicate K003837.
How does its category compare?
All JAA devicesJAA System, X-Ray, Fluoroscopic, Image-Intensified: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · JAA
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JAA
89in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JAA
4in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JAA
33in 2025
MAUDE reports naming product code JAA, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 1 | — | 35 | 9,517 |
| 2008 | 6 | 18 | 21 | 9,484 |
| 2009 | 0 | — | 18 | 12,040 |
| 2010 | 1 | — | 6 | 5,803 |
| 2011 | 4 | 48 | 7 | 14,000 |
| 2012 | 1 | — | 2 | 11,684 |
| 2013 | 6 | 129 | 3 | 13,706 |
| 2014 | 6 | 276 | 1 | 10,265 |
| 2015 | 3 | 197 | 1 | 2,922 |
| 2016 | 2 | — | 7 | 35 |
| 2017 | 1 | — | 3 | 56 |
| 2018 | 3 | 30 | 1 | 36 |
| 2019 | 6 | 49 | 2 | 49 |
| 2020 | 4 | 39 | 2 | 39 |
| 2021 | 6 | 104 | 2 | 35 |
| 2022 | 1 | — | 5 | 34 |
| 2023 | 2 | — | 9 | 41 |
| 2024 | 3 | 89 | 2 | 25 |
| 2025 | 2 | — | 4 | 33 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Centrion 500 C-Arm System is designed to provide fluoroscopic and spot-film imaging of the patient during diagnostic and surgical procedures. Clinical applications include, but are not limited to, general surgery, gastro-intestinal, urologic, orthopedic,neurologic, vascular, and emergency room procedures. The system may be used for other imaging applications at the physician's discretion.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K050866 · printed Nov 6, 2026
Cite this page
510(k) Report. “K050866: Centrion 500 C-Arm System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K050866
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Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Lineage and recalls computed Nov 3, 2026
- Page last updated Nov 3, 2026