510(k) · Cleared
ClearedIntrepid Spinal System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Medtronic Sofamor Danek · OVD Intervertebral Fusion Device With Integrated Fixation, Lumbar
Cleared on Nov 17, 2009 as substantially equivalent to K080083 (Medtronic Sofamor Danek, 2008) after a 152-day review. Its family tree reaches back 10 generations to 1984. 1 of the 751 devices in its family, counting itself, has a Class I recall. 719 later devices descend from it.
- Decided
- Nov 17, 2009
- Review
- 152 days
- Class
- Class II
- Product code
- OVD
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 10 generations to K841189 (1984). 31 ancestors in all. 719 later devices descend from it, 8 citing it directly. 1 of the 751 devices in this family, counting this one, has a Class I recall.
- Root · 10 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 6 generations between
- 3 generations backK062759 Paramount VBR SystemInnovative Spinal Technologies, Inc. · 2007
- 2 generations backK072120 Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc. · 2007
- 1 generation backK080083 Intrepid Spinal SystemMedtronic Sofamor Danek · 2008 · Recalled
- This deviceK091813 Intrepid Spinal SystemMedtronic Sofamor Danek · 2009
- Descendant · cites it directly · 718 of its ownK110063 Sovereign Spinal SystemMedtronic Sofamor Danek, Inc. · 2011
- Descendant · 2 generations on · 638 of its ownK120869 Anchor-L Lumbar CageStryker Spine · 2012
- Descendant · 3 generations on · 636 of its ownK143163 AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers…Stryker Corporation · 2015
- Descendant · 4 generations on · 469 of its ownK143616 AccuLIF TL and PL CageStryker Corporation · 2015 · Recalled
- Descendant · 4 generations on · 448 of its ownK152304 Tritanium PL CageStryker · 2015 · Recalled
Show all 10 generations
- Root · 10 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 9 generations backK990148 Stackable Cage SystemDepuy Motech Acromed · 1999
- 8 generations backK003043 Surgical Titanium Mesh SystemDepuyacromed · 2001
- 7 generations backK022793 Tetris Spinal ImplantSignus Medical, LLC · 2003
- 6 generations backK031757 Peek Tetris Spinal ImplantSignus Medical, LLC · 2003
- 5 generations backK041888 Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH · 2004
- 4 generations backK042930 Spacevision Cage SystemSpine Vision, Inc. · 2004
- 3 generations backK062759 Paramount VBR SystemInnovative Spinal Technologies, Inc. · 2007
- 2 generations backK072120 Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc. · 2007
- 1 generation backK080083 Intrepid Spinal SystemMedtronic Sofamor Danek · 2008 · Recalled
- This deviceK091813 Intrepid Spinal SystemMedtronic Sofamor Danek · 2009
Showing 5 of 719 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K211616 ExcelsiusHub5 generations on · 2021
Most influential descendants
Showing 5 of 719 · See all- K110063Sovereign Spinal SystemMedtronic Sofamor Danek, Inc. · 2011 · cites it directly718descendants
- K120869Anchor-L Lumbar CageStryker Spine · 2012 · 2 generations on638descendants
- K143163AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK Spacer…Stryker Corporation · 2015 · 3 generations on636descendants
- K143616AccuLIF TL and PL CageStryker Corporation · 2015 · 4 generations on469descendants
- K152304Tritanium PL CageStryker · 2015 · 4 generations on448descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −10 | K841189 | Oec/Rezaian Spinal Fixator | Orthopedic Equipment Co., Inc. | 1984 | — |
| −9 | K990148 | Stackable Cage System | Depuy Motech Acromed | 1999 | — |
| −8 | K003043 | Surgical Titanium Mesh System | Depuyacromed | 2001 | — |
| −7 | K022793 | Tetris Spinal Implant | Signus Medical, LLC | 2003 | — |
| −6 | K031757 | Peek Tetris Spinal Implant | Signus Medical, LLC | 2003 | — |
| −5 | K041888 | Curved Peek Tetris Spinal Implant | Signus Medizintechnik GmbH | 2004 | — |
| −4 | K042930 | Spacevision Cage System | Spine Vision, Inc. | 2004 | — |
| −3 | K062759 | Paramount VBR System | Innovative Spinal Technologies, Inc. | 2007 | — |
| −2 | K072120 | Paramount Intervertebral Body Fusion Device | Innovative Spinal Technologies, Inc. | 2007 | — |
| −1 | K080083 | Intrepid Spinal System | Medtronic Sofamor Danek | 2008 | 8 |
| 0 (this device) | K091813 | Intrepid Spinal System | Medtronic Sofamor Danek | 2009 | — |
| +1 | K110063 | Sovereign Spinal System | Medtronic Sofamor Danek, Inc. | 2011 | — |
| +2 | K120869 | Anchor-L Lumbar Cage | Stryker Spine | 2012 | — |
| +3 | K143163 | AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK… | Stryker Corporation | 2015 | — |
| +4 | K143616 | AccuLIF TL and PL Cage | Stryker Corporation | 2015 | 4 |
| +4 | K152304 | Tritanium PL Cage | Stryker | 2015 | 1 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 2 | 0 |
| 1999 | 2 | 0 |
| 2000 | 1 | 0 |
| 2001 | 3 | 0 |
| 2002 | 4 | 0 |
| 2003 | 2 | 0 |
| 2004 | 4 | 0 |
| 2005 | 1 | 0 |
| 2007 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2012 | 2 | 0 |
| 2013 | 1 | 0 |
| 2014 | 5 | 0 |
| 2015 | 10 | 0 |
| 2016 | 21 | 0 |
| 2017 | 43 | 0 |
| 2018 | 45 | 0 |
| 2019 | 61 | 0 |
| 2020 | 76 | 0 |
| 2021 | 66 | 1 |
| 2022 | 70 | 0 |
| 2023 | 88 | 0 |
| 2024 | 91 | 0 |
| 2025 | 74 | 0 |
| 2026 | 65 | 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.
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 OVD device
- #1 K222009 aprevo® anterior lumbar interbody fusion…score 26.0 · 23 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 |
|---|---|---|---|
| * | K080083 | Intrepid Spinal SystemSummary page 2…sk analysis was provided which demonstrated the subject intervertebral devices to be substantially equivalent to INTREPID™ Spinal System compouents previously cleared in K080083 (SE 04/10/2008). Minor changes have been made to the Information for Use labeling. These changes consist of modified indications,… | 2008 |
What descends from it? (719)
See all 7198 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K110063 | Sovereign Spinal System | 2011 | 718 |
| K122037 | Anatomic Peek Cervical Fusion System Cornerstone PSR Cervical Fusion System Peek Prevail… | 2013 | 281 |
| K121982 | Sovereign Spinal System | 2012 | 155 |
| K212524 | Anteralign Spinal System with Titan nanoLOCK Surface Technology | 2021 | 55 |
| K172328 | SOVEREIGN™ Spinal System | 2017 | 30 |
| K192502 | Anatomic PEEK™ Cervical Fusion System, Anatomic PEEK™ PTC Cervical Fusion System… | 2020 | 4 |
| K212653 | Catalyft LS Expandable Interbody System | 2021 | 2 |
| K241992 | Catalyft™ LS Expandable Interbody System | 2024 | 0 |
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.
- K211616ExcelsiusHubGlobus Medical, Inc. · 2021 · 5 generations on · ◆ in the 2021 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 25 years and passes through 8 companies; a new generation was cleared every 1.6 years on median.
- 6 of the 31 ancestors have a recall of any class.
- Of its descendants, K110063 (Medtronic Sofamor Danek, Inc., 2011) has gone furthest, with 718 descendants of its own.
- 2 other devices also cite its predicate K080083.
How does its category compare?
All OVD devicesOVD Intervertebral Fusion Device With Integrated Fixation, Lumbar: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.
FDA decisions per year · OVD
10in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · OVD
100in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · OVD
1in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · OVD
50in 2025
MAUDE reports naming product code OVD, 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 | — | 0 | 0 |
| 2008 | 8 | 84 | 0 | 0 |
| 2009 | 3 | 152 | 0 | 2 |
| 2010 | 8 | 117 | 0 | 2 |
| 2011 | 9 | 167 | 0 | 6 |
| 2012 | 10 | 78 | 0 | 16 |
| 2013 | 11 | 137 | 4 | 17 |
| 2014 | 14 | 139 | 0 | 35 |
| 2015 | 12 | 166 | 0 | 43 |
| 2016 | 13 | 127 | 1 | 55 |
| 2017 | 12 | 127 | 0 | 72 |
| 2018 | 14 | 126 | 0 | 112 |
| 2019 | 12 | 91 | 0 | 171 |
| 2020 | 14 | 91 | 0 | 203 |
| 2021 | 7 | 108 | 1 | 221 |
| 2022 | 14 | 133 | 1 | 74 |
| 2023 | 12 | 92 | 0 | 67 |
| 2024 | 12 | 110 | 0 | 92 |
| 2025 | 10 | 100 | 1 | 50 |
| 2026 | 8 | 93 | 1 | — |
What is it indicated for?
The SOVEREIGN™ Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc discasc (DDD) at one or two contiguous kevels from L2 to S1. DOD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should be skeletally mature and have had six menths of non-operative treatment. These implants may be inplanted via a laparoscopic or an open anterior…
Read the full statement (172 words)
The SOVEREIGN™ Spinal System is indicated for use with autogenous bone graft in patients with degenerative disc discasc (DDD) at one or two contiguous kevels from L2 to S1. DOD is defined as discogenic back pain with degeneration of the disc confirmed by history and radiographic studies. These patients should be skeletally mature and have had six menths of non-operative treatment. These implants may be inplanted via a laparoscopic or an open anterior approach.
The SOVERGIGN™ interbody device may be used as a stand-alone device or in conjunction with supplemental fixation. When used as a stand-alone device, the SOVEREIGNT™ interbody device is intended 10 be used with the three titanium alloy screws and the accompanying cover plate. I the physician chooses 1o usé less than three or none of the provided screws, then additional supplemental fixation which has been cleared by the FDA for use in the lumbar spine must be used to augment stability. The accampanying cover plate MUST be used anytime the device is used with any number of screws.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K091813 · printed Nov 4, 2026
Cite this page
510(k) Report. “K091813: Intrepid Spinal System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K091813
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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