510(k) · Cleared
ClearedReliance Cervical IBF System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Reliance Medical Systems, LLC · ODP Intervertebral Fusion Device With Bone Graft, Cervical
Cleared on Jun 9, 2015 as substantially equivalent to K120396 (Reliance Medical Systems, LLC, 2012) and 2 other predicates after a 298-day review. Its family tree reaches back 15 generations to 1984. 23 later devices descend from it.
- Decided
- Jun 9, 2015
- Review
- 298 days
- Class
- Class II
- Product code
- ODP
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 15 generations to K841189 (1984). 160 ancestors in all, the oldest K792352 (1979). 23 later devices descend from it, 4 citing it directly.
- Root · 15 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 11 generations between
- 3 generations backK100043 Coroent XLR Standalone SystemNuvasive, Inc. · 2010
- 2 generations backK102547 Coroent Interlock SystemNuvasive, Inc. · 2011
- 1 generation backK131429 Reliance Cervical Ibf SystemReliance Medical Systems, LLC · 2013
- This deviceK142269 Reliance Cervical IBF SystemReliance Medical Systems, LLC · 2015
- Descendant · cites it directly · 16 of its ownK172489 Reliance Cervical IBF SystemReliance Medical Systems, LLC · 2017
- Descendant · cites it directly · 15 of its ownK173102 Reliance Cervical IBF SystemReliance Medical Systems, LLC · 2017
- Descendant · 2 generations on · 6 of its ownK212358 Romero Cervical CageSpineup, Inc. · 2022
- Descendant · 2 generations on · 6 of its ownK212715 Vy Spine ClariVy Cervical IBF SystemVy Spine, LLC · 2021
- Descendant · cites it directly · 5 of its ownK161809 ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. · 2016
Show all 15 generations
- Root · 15 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 14 generations backK990148 Stackable Cage SystemDepuy Motech Acromed · 1999
- 13 generations backK003043 Surgical Titanium Mesh SystemDepuyacromed · 2001
- 12 generations backK022793 Tetris Spinal ImplantSignus Medical, LLC · 2003
- 11 generations backK031757 Peek Tetris Spinal ImplantSignus Medical, LLC · 2003
- 10 generations backK041888 Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH · 2004
- 9 generations backK042930 Spacevision Cage SystemSpine Vision, Inc. · 2004
- 8 generations backK062759 Paramount VBR SystemInnovative Spinal Technologies, Inc. · 2007
- 7 generations backK072120 Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc. · 2007
- 6 generations backK080083 Intrepid Spinal SystemMedtronic Sofamor Danek · 2008 · Recalled
- 5 generations backK073109 Stalif TT Intervertebral Body Fusion SystemSurgicraft, Ltd. · 2008
- 4 generations backK081849 Blackstone Pillar SA Partial Vertebral Body Replacement DeviceBlackstone Medical, Inc. · 2008 · Recalled
- 3 generations backK100043 Coroent XLR Standalone SystemNuvasive, Inc. · 2010
- 2 generations backK102547 Coroent Interlock SystemNuvasive, Inc. · 2011
- 1 generation backK131429 Reliance Cervical Ibf SystemReliance Medical Systems, LLC · 2013
- This deviceK142269 Reliance Cervical IBF SystemReliance Medical Systems, LLC · 2015
Showing 5 of 23 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 23 · See all- K172489Reliance Cervical IBF SystemReliance Medical Systems, LLC · 2017 · cites it directly16descendants
- K173102Reliance Cervical IBF SystemReliance Medical Systems, LLC · 2017 · cites it directly15descendants
- K212358Romero Cervical CageSpineup, Inc. · 2022 · 2 generations on6descendants
- K212715Vy Spine ClariVy Cervical IBF SystemVy Spine, LLC · 2021 · 2 generations on6descendants
- K161809ShurFit CpTi-HA ACIF Interbody Fusion SystemPrecision Spine, Inc. · 2016 · cites it directly5descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −15 | K841189 | Oec/Rezaian Spinal Fixator | Orthopedic Equipment Co., Inc. | 1984 | — |
| −14 | K990148 | Stackable Cage System | Depuy Motech Acromed | 1999 | — |
| −13 | K003043 | Surgical Titanium Mesh System | Depuyacromed | 2001 | — |
| −12 | K022793 | Tetris Spinal Implant | Signus Medical, LLC | 2003 | — |
| −11 | K031757 | Peek Tetris Spinal Implant | Signus Medical, LLC | 2003 | — |
| −10 | K041888 | Curved Peek Tetris Spinal Implant | Signus Medizintechnik GmbH | 2004 | — |
| −9 | K042930 | Spacevision Cage System | Spine Vision, Inc. | 2004 | — |
| −8 | K062759 | Paramount VBR System | Innovative Spinal Technologies, Inc. | 2007 | — |
| −7 | K072120 | Paramount Intervertebral Body Fusion Device | Innovative Spinal Technologies, Inc. | 2007 | — |
| −6 | K080083 | Intrepid Spinal System | Medtronic Sofamor Danek | 2008 | 8 |
| −5 | K073109 | Stalif TT Intervertebral Body Fusion System | Surgicraft, Ltd. | 2008 | — |
| −4 | K081849 | Blackstone Pillar SA Partial Vertebral Body Replacement Device | Blackstone Medical, Inc. | 2008 | 1 |
| −3 | K100043 | Coroent XLR Standalone System | Nuvasive, Inc. | 2010 | — |
| −2 | K102547 | Coroent Interlock System | Nuvasive, Inc. | 2011 | — |
| −1 | K131429 | Reliance Cervical Ibf System | Reliance Medical Systems, LLC | 2013 | — |
| 0 (this device) | K142269 | Reliance Cervical IBF System | Reliance Medical Systems, LLC | 2015 | — |
| +1 | K172489 | Reliance Cervical IBF System | Reliance Medical Systems, LLC | 2017 | — |
| +1 | K173102 | Reliance Cervical IBF System | Reliance Medical Systems, LLC | 2017 | — |
| +2 | K212358 | Romero Cervical Cage | Spineup, Inc. | 2022 | — |
| +2 | K212715 | Vy Spine ClariVy Cervical IBF System | Vy Spine, LLC | 2021 | — |
| +1 | K161809 | ShurFit CpTi-HA ACIF Interbody Fusion System | Precision Spine, Inc. | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1979 | 1 | 0 |
| 1980 | 1 | 0 |
| 1990 | 1 | 0 |
| 1992 | 2 | 0 |
| 1993 | 1 | 0 |
| 1995 | 1 | 0 |
| 1996 | 6 | 0 |
| 1997 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 2 | 0 |
| 2000 | 2 | 0 |
| 2001 | 12 | 0 |
| 2002 | 10 | 0 |
| 2003 | 13 | 0 |
| 2004 | 20 | 0 |
| 2005 | 10 | 0 |
| 2006 | 8 | 0 |
| 2007 | 10 | 0 |
| 2008 | 18 | 0 |
| 2009 | 11 | 0 |
| 2010 | 4 | 0 |
| 2011 | 4 | 0 |
| 2012 | 4 | 0 |
| 2013 | 1 | 0 |
| 2014 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
| 2017 | 3 | 0 |
| 2021 | 3 | 0 |
| 2022 | 5 | 0 |
| 2023 | 4 | 0 |
| 2024 | 2 | 0 |
| 2025 | 3 | 0 |
| 2026 | 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 ODP? 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 ODP device
- #1 K222276 CONDUIT Cages; FIBERGRAFT BG Puttyscore 53.4 · 25 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (3)
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 |
|---|---|---|---|
| * | K120396 | Reliance Cervical Ibf SystemSummary page 4…ode: OVE, ODP Substantial Equivalence The Reliance Cervical IBF is substantially equivalent to the legally marketed Reliance Cervical IBF (K120396 and K131429). The primary predicate is the Reliance Cervical IBF (K120396). Arena-C® HA PEEK Cervical Intervertebral Body Fusion… | 2012 |
| * | K131429 | Reliance Cervical Ibf SystemSummary page 4…OVE, ODP Substantial Equivalence The Reliance Cervical IBF is substantially equivalent to the legally marketed Reliance Cervical IBF (K120396 and K131429). The primary predicate is the Reliance Cervical IBF (K120396). Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device clear… | 2013 |
| * | K142026 | Spinefrontier Arena-C HA Peek Cervical Intervertebral Body Fusion Device Cleared while this submission was under review Summary page 4…Cervical IBF (K120396 and K131429). The primary predicate is the Reliance Cervical IBF (K120396). Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device cleared in K142026 is an additional predicate device. The Reliance Cervical IBF is substantially equivalent to itself in terms of material, strength… | 2014 |
What descends from it? (23)
See all 234 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 31 years and passes through 12 companies; a new generation was cleared every 1.0 years on median.
- 26 of the 160 ancestors have a recall of any class.
- Of its descendants, K172489 (Reliance Medical Systems, LLC, 2017) has gone furthest, with 16 descendants of its own.
- 4 other devices also cite its predicate K120396.
How does its category compare?
All ODP devicesODP Intervertebral Fusion Device With Bone Graft, Cervical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.
FDA decisions per year · ODP
11in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · ODP
87in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · ODP
2in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · ODP
57in 2025
MAUDE reports naming product code ODP, 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 | 0 |
| 2008 | 8 | 89 | 0 | 2 |
| 2009 | 12 | 127 | 1 | 21 |
| 2010 | 9 | 151 | 0 | 54 |
| 2011 | 25 | 113 | 1 | 38 |
| 2012 | 17 | 93 | 0 | 92 |
| 2013 | 18 | 187 | 1 | 78 |
| 2014 | 26 | 118 | 0 | 43 |
| 2015 | 24 | 180 | 0 | 51 |
| 2016 | 17 | 112 | 0 | 37 |
| 2017 | 33 | 104 | 0 | 39 |
| 2018 | 25 | 133 | 0 | 51 |
| 2019 | 22 | 92 | 0 | 141 |
| 2020 | 14 | 89 | 1 | 86 |
| 2021 | 18 | 121 | 0 | 161 |
| 2022 | 12 | 92 | 0 | 50 |
| 2023 | 34 | 165 | 0 | 36 |
| 2024 | 10 | 76 | 0 | 55 |
| 2025 | 11 | 87 | 2 | 57 |
| 2026 | 19 | 117 | 0 | — |
What is it indicated for?
The RELIANCE CERVICAL IBF System is indicated for intervertebral body fusion of the spme in skeletally mature patients. The device systems are designed for use with autogenous bone graft to facilitate fusion. One device may be used per mntervertebral space. The Reliance Cervical IBF and Rehiance Cervical IBF-HA implants are intended to be used with legally cleared supplemental spmal fixation cleared for the implanted level. The RELIANCE CERVICAL IBF…
Read the full statement (127 words)
The RELIANCE CERVICAL IBF System is indicated for intervertebral body fusion of the spme in skeletally mature patients. The device systems are designed for use with autogenous bone graft to facilitate fusion. One device may be used per mntervertebral space. The Reliance Cervical IBF and Rehiance Cervical IBF-HA implants are intended to be used with legally cleared supplemental spmal fixation cleared for the implanted level.
The RELIANCE CERVICAL IBF System is intended for use at one level in the cervical spine, from C3 to T1, for treatment of cervical disc disease (defined at neck pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies). The RELIANCE CERVICAL IBF System is to be used in patients who have six weeks of non-operative treatment.
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/K142269 · printed Nov 5, 2026
Cite this page
510(k) Report. “K142269: Reliance Cervical IBF System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K142269
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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