510(k) · Cleared
ClearedSpinefrontier Arena-C HA Peek Cervical Intervertebral Body Fusion Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Spinefrontier, Inc. · ODP Intervertebral Fusion Device With Bone Graft, Cervical
Cleared on Oct 20, 2014 as substantially equivalent to K113518 (Spinefrontier, Inc., 2012) and 2 other predicates after an 87-day review. Its family tree reaches back 9 generations to 1984. 190 later devices descend from it.
- Decided
- Oct 20, 2014
- Review
- 87 days
- Class
- Class II
- Product code
- ODP
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 9 generations to K841189 (1984). 35 ancestors in all. 190 later devices descend from it, 7 citing it directly.
- Root · 9 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 5 generations between
- 3 generations backK043479 MC+ Partial VBRLdr Spine USA · 2005
- 2 generations backK090064 Eminent Spine Interbody Fusion SystemEminent Spine · 2009 · Recalled
- 1 generation backK113518 Arena-C Cervical Intervertebral Body Fusion SystemSpinefrontier, Inc. · 2012
- This deviceK142026 Spinefrontier Arena-C HA Peek Cervical Intervertebral Body Fusion…Spinefrontier, Inc. · 2014
- Descendant · cites it directly · 108 of its ownK152515 TOMCAT Cervical Spinal SystemChoicespine, LP · 2015
- Descendant · 2 generations on · 103 of its ownK170953 Tomcat Cervical Spinal SystemChoicespine, LP · 2017
- Descendant · 3 generations on · 67 of its ownK202812 IdentiTi Cervical Standalone Interbody SystemAlphatec Spine, Inc. · 2020
- Descendant · 4 generations on · 59 of its ownK203742 IdentiTi ALIF Standalone Interbody SystemAlphatec Spine, Inc. · 2021
- Descendant · cites it directly · 50 of its ownK153615 NeoFuse HA Enhanced PLIF/TLIFHt Medical, LLC · 2016
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 backK033109 Ellys and Aurys Vertebral Body ReplacementsScient'X · 2004
- 3 generations backK043479 MC+ Partial VBRLdr Spine USA · 2005
- 2 generations backK090064 Eminent Spine Interbody Fusion SystemEminent Spine · 2009 · Recalled
- 1 generation backK113518 Arena-C Cervical Intervertebral Body Fusion SystemSpinefrontier, Inc. · 2012
- This deviceK142026 Spinefrontier Arena-C HA Peek Cervical Intervertebral Body Fusion…Spinefrontier, Inc. · 2014
Showing 5 of 190 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 190 · See all- K152515TOMCAT Cervical Spinal SystemChoicespine, LP · 2015 · cites it directly108descendants
- K170953Tomcat Cervical Spinal SystemChoicespine, LP · 2017 · 2 generations on103descendants
- K202812IdentiTi Cervical Standalone Interbody SystemAlphatec Spine, Inc. · 2020 · 3 generations on67descendants
- K203742IdentiTi ALIF Standalone Interbody SystemAlphatec Spine, Inc. · 2021 · 4 generations on59descendants
- K153615NeoFuse HA Enhanced PLIF/TLIFHt Medical, LLC · 2016 · cites it directly50descendants
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 | K033109 | Ellys and Aurys Vertebral Body Replacements | Scient'X | 2004 | — |
| −3 | K043479 | MC+ Partial VBR | Ldr Spine USA | 2005 | — |
| −2 | K090064 | Eminent Spine Interbody Fusion System | Eminent Spine | 2009 | 1 |
| −1 | K113518 | Arena-C Cervical Intervertebral Body Fusion System | Spinefrontier, Inc. | 2012 | — |
| 0 (this device) | K142026 | Spinefrontier Arena-C HA Peek Cervical Intervertebral Body Fusion Device | Spinefrontier, Inc. | 2014 | — |
| +1 | K152515 | TOMCAT Cervical Spinal System | Choicespine, LP | 2015 | — |
| +2 | K170953 | Tomcat Cervical Spinal System | Choicespine, LP | 2017 | — |
| +3 | K202812 | IdentiTi Cervical Standalone Interbody System | Alphatec Spine, Inc. | 2020 | — |
| +4 | K203742 | IdentiTi ALIF Standalone Interbody System | Alphatec Spine, Inc. | 2021 | — |
| +1 | K153615 | NeoFuse HA Enhanced PLIF/TLIF | Ht Medical, LLC | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 2 | 0 |
| 1999 | 2 | 0 |
| 2000 | 1 | 0 |
| 2001 | 8 | 0 |
| 2002 | 4 | 0 |
| 2003 | 1 | 0 |
| 2004 | 3 | 0 |
| 2005 | 1 | 0 |
| 2008 | 3 | 0 |
| 2011 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2015 | 2 | 0 |
| 2016 | 2 | 0 |
| 2017 | 7 | 0 |
| 2018 | 7 | 0 |
| 2019 | 5 | 0 |
| 2020 | 10 | 0 |
| 2021 | 11 | 0 |
| 2022 | 19 | 0 |
| 2023 | 35 | 0 |
| 2024 | 32 | 0 |
| 2025 | 31 | 0 |
| 2026 | 29 | 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 |
|---|---|---|---|
| * | K113518 | Arena-C Cervical Intervertebral Body Fusion SystemSummary page 6…indications for use for the Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device is identical to that of the Arena-C® Cervical Intervertebral Body Fusion System (K113518). TECHNOLOGICAL CHARACTERISTICS The SpineFrontier Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device was shown to be su… | 2012 |
| * | K090064 | Eminent Spine Interbody Fusion SystemSummary page 6…usion System SpineFrontier Table 5-2 Additional Predicate Devices 510k Number Trade or Proprietary or Model Name Manufacturer K090064 Interbody Fusion System (Copperhead) Eminent Spine K110733 Daytona Anterior Cervic… | 2009 |
| * | K110733 | Daytona Anterior Cervical CageSummary page 6…Trade or Proprietary or Model Name Manufacturer K090064 Interbody Fusion System (Copperhead) Eminent Spine K110733 Daytona Anterior Cervical Cage SpineNet SpineFrontier Arena-C® HA Cervical Interverte… | 2011 |
What descends from it? (190)
See all 1907 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K152515 | TOMCAT Cervical Spinal System | 2015 | 108 |
| K153615 | NeoFuse HA Enhanced PLIF/TLIF | 2016 | 50 |
| K173324 | ALTA Anterior Cervical Interbody Spacer | 2018 | 27 |
| K142269 | Reliance Cervical IBF System | 2015 | 23 |
| K172484 | A-CIFT SoloFuse | 2018 | 7 |
| K161809 | ShurFit CpTi-HA ACIF Interbody Fusion System | 2016 | 5 |
| K180674 | EVOL® ha-C Cervical Interbody Fusion System | 2018 | 3 |
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 30 years and passes through 8 companies; a new generation was cleared every 1.9 years on median.
- 7 of the 35 ancestors have a recall of any class.
- Of its descendants, K152515 (Choicespine, LP, 2015) has gone furthest, with 108 descendants of its own.
- 1 other device also cites its predicate K113518.
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. 2014, 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 SpineFrontier Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device is a spinal intervertebral body fusion device intended for intervertebral body fusion of the spine of skeletally mature patients, using autogenous bone graft to facilitate fusion. The device is indicated for use in patients with degenerative disc disease (DDD) of the cervical spine at one disc level from the C2-C3 disc to the C7-T1 disc. The SpineFrontier® Arena-C® HA PEEK…
Read the full statement (138 words)
The SpineFrontier Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device is a spinal intervertebral body fusion device intended for intervertebral body fusion of the spine of skeletally mature patients, using autogenous bone graft to facilitate fusion. The device is indicated for use in patients with degenerative disc disease (DDD) of the cervical spine at one disc level from the C2-C3 disc to the C7-T1 disc.
The SpineFrontier® Arena-C® HA PEEK Cervical Intervertebral Body Fusion Device is intended to be used with supplemental spinal fixation system(s) cleared for use in the cervical spine (example: Anterior Cervical Plate Fixation).
Degenerative disc disease is defined as discogenic pain with degeneration of the disc confirmed by history or radiographic studies. These patients should be skeletally mature and have had six (6) weeks of non-operative treatment prior to treatment with an intervertebral cage.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K142026 · printed Nov 6, 2026
Cite this page
510(k) Report. “K142026: Spinefrontier Arena-C HA Peek Cervical Intervertebral Body Fusion Device.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K142026
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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