510(k) · Cleared
ClearedDSM Biomedical DPR Cable
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Dsm Biomedical · JDQ Cerclage, Fixation
Cleared on Oct 29, 2015 as substantially equivalent to K920201 (Sofamor Danek Mfg., Inc., 1992) after a 304-day review. Its family tree reaches back 1 generation to 1992. 7 later devices descend from it.
- Decided
- Oct 29, 2015
- Review
- 304 days
- Class
- Class II
- Product code
- JDQ
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 1 generation to K920201 (1992). 7 later devices descend from it, 2 citing it directly.
- Root · 1 generation backK920201 Titanium Alloy Songer Cable SystemSofamor Danek Mfg., Inc. · 1992
- This deviceK143716 DSM Biomedical DPR CableDsm Biomedical · 2015
- Descendant · cites it directly · 5 of its ownK170206 Arthrex FiberTape CerclageArthrex, Inc. · 2017
- Descendant · 2 generations on · 2 of its ownK232755 Arthrex FiberTape and TigerTape Cerclage SuturesArthrex, Inc. · 2023
- Descendant · cites it directly · 1 of its ownK230976 Arthrex Radiopaque FiberTape Cerclage suturesArthrex, Inc. · 2023
- Descendant · 2 generations on · 0 of its ownK260018 Arthrex FiberButtonArthrex, Inc. · 2026
- Descendant · 3 generations on · 0 of its ownK243344 Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque…Arthrex, Inc. · 2025
Showing 5 of 7 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 7 · See all- K170206Arthrex FiberTape CerclageArthrex, Inc. · 2017 · cites it directly5descendants
- K232755Arthrex FiberTape and TigerTape Cerclage SuturesArthrex, Inc. · 2023 · 2 generations on2descendants
- K230976Arthrex Radiopaque FiberTape Cerclage suturesArthrex, Inc. · 2023 · cites it directly1descendant
- K260018Arthrex FiberButtonArthrex, Inc. · 2026 · 2 generations on0descendants
- K243344Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape Cerclage…Arthrex, Inc. · 2025 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −1 | K920201 | Titanium Alloy Songer Cable System | Sofamor Danek Mfg., Inc. | 1992 | — |
| 0 (this device) | K143716 | DSM Biomedical DPR Cable | Dsm Biomedical | 2015 | — |
| +1 | K170206 | Arthrex FiberTape Cerclage | Arthrex, Inc. | 2017 | — |
| +2 | K232755 | Arthrex FiberTape and TigerTape Cerclage Sutures | Arthrex, Inc. | 2023 | — |
| +1 | K230976 | Arthrex Radiopaque FiberTape Cerclage sutures | Arthrex, Inc. | 2023 | — |
| +2 | K260018 | Arthrex FiberButton | Arthrex, Inc. | 2026 | — |
| +3 | K243344 | Arthrex FiberTape and TigerTape Cerclage Sutures; Arthrex Radiopaque FiberTape… | Arthrex, Inc. | 2025 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 1 | 0 |
| 2023 | 3 | 0 |
| 2025 | 2 | 0 |
| 2026 | 1 | 0 |
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 JDQ? 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 JDQ device
- #1 K261271 Cable-Ready® Cable Grip Systemscore 14.7 · 11 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 |
|---|---|---|---|
| * | K920201 | Titanium Alloy Songer Cable SystemSummary page 4…gery Predicate: Titanium Alloy Songer Cable System/ Atlas Cable System (Medtronic Sofamor Danek , K920201) Reference Devices: Iso-Elastic Cable (Kinamed Inc., K102834) Orth… | 1992 |
| † | K102834 | Iso-Elastic Cerclage System (1MM and 2MM Cable Diameter) | 2011 |
| † | K924141 | Orthopaedic Polyethylene Cable | 1993 |
What descends from it? (7)
2 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
No FDA recall names this device.
No ancestor or descendant has a Class I recall.
What does this lineage say?
How does its category compare?
All JDQ devicesJDQ Cerclage, Fixation: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · JDQ
2in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · JDQ
130in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · JDQ
5in 2019
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JDQ
84in 2025
MAUDE reports naming product code JDQ, 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 | — | 0 | 5 |
| 2008 | 2 | — | 2 | 25 |
| 2009 | 2 | — | 0 | 19 |
| 2010 | 0 | — | 2 | 28 |
| 2011 | 6 | 130 | 0 | 30 |
| 2012 | 3 | 134 | 0 | 130 |
| 2013 | 1 | — | 1 | 321 |
| 2014 | 2 | — | 0 | 223 |
| 2015 | 5 | 92 | 1 | 205 |
| 2016 | 4 | 129 | 0 | 224 |
| 2017 | 1 | — | 0 | 138 |
| 2018 | 6 | 101 | 0 | 182 |
| 2019 | 0 | — | 5 | 158 |
| 2020 | 4 | 93 | 0 | 125 |
| 2021 | 0 | — | 0 | 141 |
| 2022 | 2 | — | 0 | 134 |
| 2023 | 3 | 141 | 0 | 98 |
| 2024 | 3 | 130 | 0 | 115 |
| 2025 | 2 | — | 0 | 84 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The DPR Cable is intended for:
Spinal applications include sublaminar and intraspinous process wiring for trauma applications.
Trochanteric reattachment after trochanteric osteotomy following total hip arthroplasty.
Sternotomy indications including the “rewiring” of osteomized sternums.
Trauma surgery indications including olecranon, ankle, patella and some shoulder fracture rewiring.
The device is intended for single patient use only.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K143716 · printed Nov 6, 2026
Cite this page
510(k) Report. “K143716: DSM Biomedical DPR Cable.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K143716
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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