510(k) · Decided
DecidedDSS Stabilization System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Paradigm Spine, LLC · NQP Posterior Metal/Polymer Spinal System, Fusion
Cleared on Jul 2, 2010 as substantially equivalent to K080241 (Paradigm Spine, LLC, 2008) and 3 other predicates after a 74-day review. Its family tree reaches back 6 generations to 1990. 2 later devices descend from it.
- Decided
- Jul 2, 2010
- Review
- 74 days
- Class
- Class II
- Product code
- NQP
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 6 generations to K901587 (1990). 27 ancestors in all. 2 later devices descend from it, 2 citing it directly.
- Root · 6 generations backK901587 TSRH Sacral L-ConnectorDanek Medical, Inc. · 1990
- 5 generations backK950099 Synergy (TM) TI Posterior Spinal SystemBuckman Co., Inc. · 1997
- 4 generations backK973836 Synergy 6.35MM SS Rod with Screws for Anterior Use, Part of the…Cross Medical Products, Inc. · 1998
- 3 generations backK080241 DDS Stabilization SystemParadigm Spine, LLC · 2008
- 2 generations backK090408 Modification to: DSS Stabilization SystemParadigm Spine, LLC · 2009
- 1 generation backK091944 Modification to: DSS Stabilization SystemParadigm Spine, LLC · 2009
- This deviceK101083 DSS Stabilization SystemParadigm Spine, LLC · 2010
- Descendant · cites it directly · 1 of its ownK113625 DSS Stabilization SystemParadigm Spine, LLC · 2012
- Descendant · cites it directly · 0 of its ownK120491 DSS Stabilization System-RigidParadigm Spine, LLC · 2012
Most influential descendants
Showing 2 of 2 · See allView FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K901587 | TSRH Sacral L-Connector | Danek Medical, Inc. | 1990 | — |
| −5 | K950099 | Synergy (TM) TI Posterior Spinal System | Buckman Co., Inc. | 1997 | — |
| −4 | K973836 | Synergy 6.35MM SS Rod with Screws for Anterior Use, Part of the Cross… | Cross Medical Products, Inc. | 1998 | — |
| −3 | K080241 | DDS Stabilization System | Paradigm Spine, LLC | 2008 | — |
| −2 | K090408 | Modification to: DSS Stabilization System | Paradigm Spine, LLC | 2009 | — |
| −1 | K091944 | Modification to: DSS Stabilization System | Paradigm Spine, LLC | 2009 | — |
| 0 (this device) | K101083 | DSS Stabilization System | Paradigm Spine, LLC | 2010 | — |
| +1 | K113625 | DSS Stabilization System | Paradigm Spine, LLC | 2012 | — |
| +1 | K120491 | DSS Stabilization System-Rigid | Paradigm Spine, LLC | 2012 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1990 | 1 | 0 |
| 1992 | 5 | 0 |
| 1993 | 2 | 0 |
| 1994 | 1 | 0 |
| 1995 | 2 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 3 | 0 |
| 2000 | 1 | 0 |
| 2005 | 1 | 0 |
| 2008 | 2 | 0 |
| 2009 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2012 | 2 | 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 NQP? 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 NQP device
- #1 K203678 CD HORIZON™ Spinal Systemscore 10.9 · 15 generations · no Class I recall
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | K080241 | DDS Stabilization SystemSummary page 2…addition of a 20mm long rigid coupler. Predicate Device(s): DSSTM Stabilization System -- Rigid was shown to be substantially equivalent to previously cleared devices (K080241, K090408. K090099. and K091944) and has the same indications for use, design, function, and materials used. Non-clinical Testing… | 2008 |
| * | K090408 | Modification to: DSS Stabilization SystemSummary page 2…of a 20mm long rigid coupler. Predicate Device(s): DSSTM Stabilization System -- Rigid was shown to be substantially equivalent to previously cleared devices (K080241, K090408. K090099. and K091944) and has the same indications for use, design, function, and materials used. Non-clinical Testing: Static… | 2009 |
| * | K090099 | DSS Stabilization SystemSummary page 2…m long rigid coupler. Predicate Device(s): DSSTM Stabilization System -- Rigid was shown to be substantially equivalent to previously cleared devices (K080241, K090408. K090099. and K091944) and has the same indications for use, design, function, and materials used. Non-clinical Testing: Static and dynam… | 2009 |
| * | K091944 | Modification to: DSS Stabilization SystemSummary page 2…coupler. Predicate Device(s): DSSTM Stabilization System -- Rigid was shown to be substantially equivalent to previously cleared devices (K080241, K090408. K090099. and K091944) and has the same indications for use, design, function, and materials used. Non-clinical Testing: Static and dynamic mechanical… | 2009 |
What descends from it? (2)
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?
- The line of descent spans 20 years and passes through 4 companies; a new generation was cleared every 1.1 years on median.
- 1 of the 27 ancestors has a recall of any class.
- Of its descendants, K113625 (Paradigm Spine, LLC, 2012) has gone furthest, with 1 descendant of its own.
- 4 other devices also cite its predicate K080241.
How does its category compare?
All NQP devicesNQP Posterior Metal/Polymer Spinal System, Fusion: FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.
FDA decisions per year · NQP
1in 2021
2026 to Oct 25, outlined.
Median 510(k) review, days · NQP
70in 2009
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · NQP
6in 2012
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · NQP
8in 2025
MAUDE reports naming product code NQP, 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 | 2 | — | 34 | 45 |
| 2008 | 6 | 156 | 4 | 101 |
| 2009 | 3 | 70 | 6 | 109 |
| 2010 | 2 | — | 0 | 119 |
| 2011 | 0 | — | 0 | 60 |
| 2012 | 0 | — | 6 | 66 |
| 2013 | 0 | — | 0 | 58 |
| 2014 | 1 | — | 0 | 46 |
| 2015 | 0 | — | 0 | 38 |
| 2016 | 0 | — | 0 | 79 |
| 2017 | 0 | — | 0 | 28 |
| 2018 | 0 | — | 0 | 29 |
| 2019 | 2 | — | 0 | 8 |
| 2020 | 0 | — | 0 | 15 |
| 2021 | 1 | — | 0 | 7 |
| 2022 | 0 | — | 0 | 12 |
| 2023 | 0 | — | 0 | 2 |
| 2024 | 0 | — | 0 | 8 |
| 2025 | 0 | — | 0 | 8 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
DSS™ Stabilization System - Rigid The DSS™ Stabilization System - Rigid is intended as a single-level system for noncervical pedicle fixation from the T4 to S1 vertebrae in skeletally mature patients to help provide immobilization and stabilization of spinal segments as an adjunct to fusion for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and…
Read the full statement (231 words)
DSS™ Stabilization System - Rigid
The DSS™ Stabilization System - Rigid is intended as a single-level system for noncervical pedicle fixation from the T4 to S1 vertebrae in skeletally mature patients to help provide immobilization and stabilization of spinal segments as an adjunct to fusion for the following indications: degenerative disc disease (defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies); spondylolisthesis; trauma (i.e., fracture or dislocation); spinal stenosis; curvatures (i.e., scoliosis, kyphosis, and/or lordosis); tumor; pseudarthrosis; and failed previous fusion. The DSS™ Stabilization System - Rigid is intended to be used with autograft and/or allograft.
DSS™ Stabilization System - Slotted
The DSS™ Stabilization System - Slotted is intended to provide immobilization and stabilization of spinal segments as an adjunct to fusion in the treatment of the following acute and chronic instabilities or deformities of the thoracic, lumbar, and sacral spine: degenerative spondylolisthesis with objective evidence of neurologic impairment, kyphosis, and failed previous fusion (pseudarthrosis).
In addition, the DSS™ Stabilization System - Slotted is indicated for use in patients:
* Who are receiving fusions with autogenous graft only;
* Who are having the device fixed or attached to the lumbar or sacral spine;
* Who are having the device removed after the development of a solid fusion mass.
Note: The Rigid Coupler and Slotted Coupler are not intended to be used together.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K101083 · printed Nov 6, 2026
Cite this page
510(k) Report. “K101083: DSS Stabilization System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K101083
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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