510(k) · Cleared
Recalled · 2008Acumed Bone Graft System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Acu Med, Inc. · KIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment
Cleared on May 7, 1996 after a 76-day review. The FDA summary names its predicate without a number. It has been recalled 2 times.
- Decided
- May 7, 1996
- Review
- 76 days
- Class
- Class I
- Product code
- KIJ
- Recalls
- 2
- Predicates
- 0
The FDA summary names its predicate without a number.
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.
Planning a device in KIJ? A 510(k) Report weighs predicate choices, recall history and review times for a new device like this one.
- Candidate predicates for a device like this, rankedin the report
- Recall history across each candidate’s familyin 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 |
|---|---|---|---|
| * | — | Wright Medical Technology’s Precision Bone Grafting System Named without a submission number |
What descends from it?
No later submission names this one as a predicate yet.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Feb 14, 2008 | Not classified | Z-2119-2008 | Packaging process control | Product sterility may be compromised. |
| Feb 14, 2008 | Not classified | Z-2118-2008 | Packaging process control | Product sterility may be compromised. |
No ancestor or descendant has a Class I recall.
How does its category compare?
All KIJ devicesKIJ Instrument, Surgical, Orthopedic, Dc-Powered Motor And Accessory/Attachment: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KIJ
1in 2016
2026 to Oct 25, outlined.
Median 510(k) review, days · KIJ
Too few KIJ 510(k)s in any year since 2007 to give a median.
Recalls per year · KIJ
10in 2008
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KIJ
4in 2025
MAUDE reports naming product code KIJ, 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 | 0 | — | 0 | 10 |
| 2008 | 0 | — | 10 | 4 |
| 2009 | 0 | — | 0 | 265 |
| 2010 | 1 | — | 0 | 424 |
| 2011 | 0 | — | 0 | 1,080 |
| 2012 | 1 | — | 0 | 615 |
| 2013 | 0 | — | 0 | 288 |
| 2014 | 0 | — | 0 | 36 |
| 2015 | 0 | — | 0 | 36 |
| 2016 | 1 | — | 0 | 11 |
| 2017 | 0 | — | 0 | 1 |
| 2018 | 0 | — | 0 | 1 |
| 2019 | 0 | — | 0 | 1 |
| 2020 | 0 | — | 0 | 1 |
| 2021 | 0 | — | 0 | 0 |
| 2022 | 0 | — | 0 | 4 |
| 2023 | 0 | — | 0 | 6 |
| 2024 | 0 | — | 0 | 8 |
| 2025 | 0 | — | 0 | 4 |
| 2026 | 0 | — | 0 | — |
https://510kreport.com/device/K960711 · printed Nov 6, 2026
Cite this page
510(k) Report. “K960711: Acumed Bone Graft System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K960711
Report an extraction error
Are you the manufacturer?
Record history
- FDA decision record loaded May 2, 2026
- Summary read Oct 13, 2026 (extraction version 9eaa42aa01ed)
- Page last updated Nov 3, 2026