510(k) · Cleared
ClearedReliance VBS System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Reliance Medical Systems, LLC · MQP Spinal Vertebral Body Replacement Device
Cleared on Jul 2, 2008 as substantially equivalent to K063637 (Reliance Medical Systems, LLC, 2007) and 18 other predicates after a 47-day review. Its family tree reaches back 9 generations to 1984.
- Decided
- Jul 2, 2008
- Review
- 47 days
- Class
- Class II
- Product code
- MQP
- Recalls
- None
- Predicates
- 19
Its longest line of descent runs back 9 generations to K841189 (1984). 51 ancestors in all. No later device cites it as a predicate yet.
- Root · 9 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 5 generations between
- 3 generations backK042930 Spacevision Cage SystemSpine Vision, Inc. · 2004
- 2 generations backK051454 Aleutian Spacer SystemK2m, LLC · 2005
- 1 generation backK063637 Reliance VBS SystemReliance Medical Systems, LLC · 2007
- This deviceK081383 Reliance VBS SystemReliance Medical Systems, LLC · 2008
Show all 9 generations
- Root · 9 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 8 generations backK990148 Stackable Cage SystemDepuy Motech Acromed · 1999
- 7 generations backK003043 Surgical Titanium Mesh SystemDepuyacromed · 2001
- 6 generations backK022793 Tetris Spinal ImplantSignus Medical, LLC · 2003
- 5 generations backK031757 Peek Tetris Spinal ImplantSignus Medical, LLC · 2003
- 4 generations backK041888 Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH · 2004
- 3 generations backK042930 Spacevision Cage SystemSpine Vision, Inc. · 2004
- 2 generations backK051454 Aleutian Spacer SystemK2m, LLC · 2005
- 1 generation backK063637 Reliance VBS SystemReliance Medical Systems, LLC · 2007
- This deviceK081383 Reliance VBS SystemReliance Medical Systems, LLC · 2008
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −9 | K841189 | Oec/Rezaian Spinal Fixator | Orthopedic Equipment Co., Inc. | 1984 | — |
| −8 | K990148 | Stackable Cage System | Depuy Motech Acromed | 1999 | — |
| −7 | K003043 | Surgical Titanium Mesh System | Depuyacromed | 2001 | — |
| −6 | K022793 | Tetris Spinal Implant | Signus Medical, LLC | 2003 | — |
| −5 | K031757 | Peek Tetris Spinal Implant | Signus Medical, LLC | 2003 | — |
| −4 | K041888 | Curved Peek Tetris Spinal Implant | Signus Medizintechnik GmbH | 2004 | — |
| −3 | K042930 | Spacevision Cage System | Spine Vision, Inc. | 2004 | — |
| −2 | K051454 | Aleutian Spacer System | K2m, LLC | 2005 | — |
| −1 | K063637 | Reliance VBS System | Reliance Medical Systems, LLC | 2007 | — |
| 0 (this device) | K081383 | Reliance VBS System | Reliance Medical Systems, LLC | 2008 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2000 | 2 | 0 |
| 2001 | 8 | 0 |
| 2002 | 6 | 0 |
| 2003 | 9 | 0 |
| 2004 | 14 | 0 |
| 2005 | 3 | 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 MQP? 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 MQP device
- #1 K261810 Vertiwedge® Intraosseous Systemscore 18.1 · 22 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (19)
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 |
|---|---|---|---|
| * | K063637 | Reliance VBS SystemSummary page 1…3060 Product Code: MQP Substantial Equivalence The Reliance VBS is substantially equivalent to the legally marketed Reliance VBS System (K063637), the Pioneer Surgical Vertebral Spacer (K043206), the Alphatec NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050… | 2007 |
| * | K043206 | Pioneer Vertebral Body Replacement Device (Pioneer Vertebral Spacer)Summary page 1…MQP Substantial Equivalence The Reliance VBS is substantially equivalent to the legally marketed Reliance VBS System (K063637), the Pioneer Surgical Vertebral Spacer (K043206), the Alphatec NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), t… | 2005 |
| * | K042201 | Novel VBR Spinal SystemSummary page 1…Reliance VBS is substantially equivalent to the legally marketed Reliance VBS System (K063637), the Pioneer Surgical Vertebral Spacer (K043206), the Alphatec NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-S… | 2004 |
| * | K050449 | Quantum Vertebral Body ReplacementSummary page 1…egally marketed Reliance VBS System (K063637), the Pioneer Surgical Vertebral Spacer (K043206), the Alphatec NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K… | 2005 |
| * | K051454 | Aleutian Spacer SystemSummary page 1…37), the Pioneer Surgical Vertebral Spacer (K043206), the Alphatec NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601… | 2005 |
| * | K041556 | Modification to Verte-Stack Spinal SystemSummary page 1…Alphatec NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO… | 2004 |
| * | K041452 | Modification to Verte-Stack Spinal SystemSummary page 1…NOVEL VBR (K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K0… | 2004 |
| * | K040536 | Modification to Verte-Stack Spinal SystemSummary page 1…(K042201), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K0… | 2004 |
| * | K040422 | Modification to Verte-StackSummary page 1…), the Quantum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). T… | 2004 |
| * | K040167 | Verte-Stack Spinal SystemSummary page 1…antum Vertebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Relian… | 2004 |
| * | K031780 | Verte-Stack Spinal SystemSummary page 1…tebral Body Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is… | 2003 |
| * | K030736 | Verte-Stack Spinal System, Extra Small SizesSummary page 1…dy Replacement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivale… | 2003 |
| * | K030735 | Modified Verte-Stack Spinal SystemSummary page 1…ement (K050449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivalent to the… | 2003 |
| * | K030601 | Verte-Stack Spinal SystemSummary page 1…50449), the K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivalent to these commer… | 2003 |
| * | K023570 | Modification to Verte-Stack Spinal SystemSummary page 1…he K2M Aleutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivalent to these commercially av… | 2002 |
| * | K021791 | Verte-Stack Spinal SystemSummary page 1…eutian Spacer System (K051454), the Medtronic Sofamor Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivalent to these commercially available d… | 2002 |
| * | K011037 | Vertebral Spacer | 2002 |
| * | K020152 | Synthes Vertebral Spacer TISummary page 1…Danek Verte-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivalent to these commercially available devices in terms of material, intended use, levels of a… | 2002 |
| * | K024364 | Synthes Vertebral Spacer TI (Curved and Narrow)Summary page 1…te-STACK System (K041556, K041452, K040536, K040422, K040167, K031780, K030736, K030735, K030601, K023570, K021791), and the Synthes Vertebral Spacer (KO I1037, K020152, K024364). The Reliance VBS is equivalent to these commercially available devices in terms of material, intended use, levels of attachment… | 2003 |
What descends from it?
No later submission names this one as a predicate yet.
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 24 years and passes through 8 companies; a new generation was cleared every 1.0 years on median.
- 3 of the 51 ancestors have a recall of any class.
How does its category compare?
All MQP devicesMQP Spinal Vertebral Body Replacement Device: FDA decisions, review times, recalls and adverse event reports over 20 years. 2008, this device’s year, is highlighted.
FDA decisions per year · MQP
4in 2024
2026 to Oct 25, outlined.
Median 510(k) review, days · MQP
187in 2024
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MQP
1in 2022
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · MQP
168in 2025
MAUDE reports naming product code MQP, 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 | 30 | 107 | 2 | 61 |
| 2008 | 17 | 47 | 0 | 76 |
| 2009 | 11 | 115 | 14 | 111 |
| 2010 | 6 | 174 | 2 | 166 |
| 2011 | 8 | 237 | 1 | 121 |
| 2012 | 7 | 82 | 2 | 141 |
| 2013 | 3 | 90 | 0 | 207 |
| 2014 | 5 | 125 | 0 | 216 |
| 2015 | 8 | 126 | 0 | 258 |
| 2016 | 0 | — | 0 | 129 |
| 2017 | 9 | 97 | 0 | 141 |
| 2018 | 6 | 152 | 0 | 130 |
| 2019 | 8 | 93 | 0 | 117 |
| 2020 | 3 | 103 | 15 | 157 |
| 2021 | 0 | — | 0 | 208 |
| 2022 | 1 | — | 1 | 137 |
| 2023 | 1 | — | 0 | 71 |
| 2024 | 4 | 187 | 0 | 98 |
| 2025 | 0 | — | 0 | 168 |
| 2026 | 3 | 102 | 0 | — |
What is it indicated for?
The Reliance VBS System is intended for use in the thoracolumbar spine (T1-L5) to replace a portion of a collapsed, damaged, or unstable vertebral body due to tumor or trauma (i.e., fracture) in order to achieve anterior decompression of the spinal cord and neural tissues, and to restore the height of a collapsed vertebral body. The Reliance VBS is designed to restore biomechanical integrity of the anterior, middle, and posterior spinal column, even in the absence of fusion for a prolonged period of time.
The Reliance VBS System is to be used with a legally cleared anterior or posterior supplemental fixation device. Additionally, the Reliance VBS is intended to be used with bone graft.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K081383 · printed Nov 4, 2026
Cite this page
510(k) Report. “K081383: Reliance VBS System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K081383
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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