510(k) · Cleared
ClearedRampart A Lumbar Interbody Fusion Device
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Spineology, Inc. · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Cleared on Feb 4, 2016 as substantially equivalent to K123652 (Spineology, Inc., 2013) and 2 other predicates after a 104-day review. Its family tree reaches back 6 generations to 2011. 28 later devices descend from it.
- Decided
- Feb 4, 2016
- Review
- 104 days
- Class
- Class II
- Product code
- MAX
- Recalls
- None
- Predicates
- 3
Its longest line of descent runs back 6 generations to K111880 (2011). 9 ancestors in all, the oldest K110933 (2011). 28 later devices descend from it, 2 citing it directly.
- Root · 6 generations backK111880 Spineolgy Peek Bullet Lumber Interbody Fusion DeviceSpineology, Inc. · 2011
- 5 generations backK113030 Spineology Peek Bullet Lumbar Interbody Fusion DeviceSpineology, Inc. · 2012
- 4 generations backK120293 Spineology Peek Lumbar Interbody Fusion DriveSpineology, Inc. · 2012
- 3 generations backK123652 Spineology Peek Lumbar Interbody Fusion DeviceSpineology, Inc. · 2013
- 2 generations backK131216 Rampart OSpineology, Inc. · 2013
- 1 generation backK132053 Rampart-O, Rampart-TSpineology, Inc. · 2013
- This deviceK153082 Rampart A Lumbar Interbody Fusion DeviceSpineology, Inc. · 2016
- Descendant · cites it directly · 27 of its ownK160906 Rampart O Lumbar Interbody Fusion Device, Rampart T Lumbar Interbody…Spineology, Inc. · 2016
- Descendant · 2 generations on · 11 of its ownK170643 Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) SystemRti Surgical, Inc. Dba Rti Biologics · 2017
- Descendant · 3 generations on · 10 of its ownK172343 Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D TechnologyRti Surgical, Inc. · 2017
- Descendant · 2 generations on · 9 of its ownK162879 Elite Expandable Interbody Fusion DeviceSpineology, Inc. · 2017
- Descendant · 3 generations on · 8 of its ownK171425 Concorde LiftMedos International SARL · 2017 · Recalled
Showing 5 of 28 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 28 · See all- K160906Rampart O Lumbar Interbody Fusion Device, Rampart T Lumbar Interbody Fusion Device…Spineology, Inc. · 2016 · cites it directly27descendants
- K170643Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) SystemRti Surgical, Inc. Dba Rti Biologics · 2017 · 2 generations on11descendants
- K172343Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D TechnologyRti Surgical, Inc. · 2017 · 3 generations on10descendants
- K162879Elite Expandable Interbody Fusion DeviceSpineology, Inc. · 2017 · 2 generations on9descendants
- K171425Concorde LiftMedos International SARL · 2017 · 3 generations on8descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K111880 | Spineolgy Peek Bullet Lumber Interbody Fusion Device | Spineology, Inc. | 2011 | — |
| −5 | K113030 | Spineology Peek Bullet Lumbar Interbody Fusion Device | Spineology, Inc. | 2012 | — |
| −4 | K120293 | Spineology Peek Lumbar Interbody Fusion Drive | Spineology, Inc. | 2012 | — |
| −3 | K123652 | Spineology Peek Lumbar Interbody Fusion Device | Spineology, Inc. | 2013 | — |
| −2 | K131216 | Rampart O | Spineology, Inc. | 2013 | — |
| −1 | K132053 | Rampart-O, Rampart-T | Spineology, Inc. | 2013 | — |
| 0 (this device) | K153082 | Rampart A Lumbar Interbody Fusion Device | Spineology, Inc. | 2016 | — |
| +1 | K160906 | Rampart O Lumbar Interbody Fusion Device, Rampart T Lumbar Interbody Fusion… | Spineology, Inc. | 2016 | — |
| +2 | K170643 | Interbody Fusion (IBF)/Vertebral Body Replacement (VBR) System | Rti Surgical, Inc. Dba Rti Biologics | 2017 | — |
| +3 | K172343 | Fortilink® Interbody Fusion (IBF) System with TETRAfuse® 3D Technology | Rti Surgical, Inc. | 2017 | — |
| +2 | K162879 | Elite Expandable Interbody Fusion Device | Spineology, Inc. | 2017 | — |
| +3 | K171425 | Concorde Lift | Medos International SARL | 2017 | 2 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2011 | 1 | 0 |
| 2012 | 1 | 0 |
| 2013 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 1 | 0 |
| 2017 | 6 | 0 |
| 2018 | 2 | 0 |
| 2019 | 6 | 0 |
| 2020 | 1 | 0 |
| 2021 | 1 | 0 |
| 2022 | 2 | 0 |
| 2023 | 2 | 0 |
| 2024 | 3 | 0 |
| 2025 | 2 | 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 MAX? 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 MAX device
- #1 K203714 NuVasive Thoracolumbar Interbody Systems…score 102.5 · 24 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 |
|---|---|---|---|
| * | K123652 | Spineology Peek Lumbar Interbody Fusion DeviceSummary page 4…y fusion device Regulation Number: 21 CFR 888.3080 Product Code: MAX Regulatory Class: Class 11 510(k) Review Panel: Orthopedic Predicate Devices Primary Predicate K123652 Spineology PEEK Lumbar Interbody Fusion Device Additional Predicates K132053 Rampart O, Rampart T Lumbar Interbody Fusion Device… | 2013 |
| * | K132053 | Rampart-O, Rampart-TSummary page 4…ory Class: Class 11 510(k) Review Panel: Orthopedic Predicate Devices Primary Predicate K123652 Spineology PEEK Lumbar Interbody Fusion Device Additional Predicates K132053 Rampart O, Rampart T Lumbar Interbody Fusion Device K121129 Spineology PEEK Lumbar Interbody Fusion Device Reference Device K072… | 2013 |
| * | K121129 | Spineology Peek Lumbar Interbody Fusion DeviceSummary page 4…ate Devices Primary Predicate K123652 Spineology PEEK Lumbar Interbody Fusion Device Additional Predicates K132053 Rampart O, Rampart T Lumbar Interbody Fusion Device K121129 Spineology PEEK Lumbar Interbody Fusion Device Reference Device K072253 SynFix-LR (Synthes Spine) Purpose of Submission The pu… | 2012 |
| † | K072253 | Synfix-LR Spacer | 2007 |
What descends from it? (28)
See all 282 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 5 years and passes through 1 company; a new generation was cleared every 4 months on median.
- None of the 9 ancestors has a recall.
- Of its descendants, K160906 (Spineology, Inc., 2016) has gone furthest, with 27 descendants of its own.
- 2 other devices also cite its predicate K123652.
How does its category compare?
All MAX devicesMAX Intervertebral Fusion Device With Bone Graft, Lumbar: FDA decisions, review times, recalls and adverse event reports over 20 years. 2016, this device’s year, is highlighted.
FDA decisions per year · MAX
29in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · MAX
85in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · MAX
5in 2025
Class I (1 since 2007) Class II/III not classified
Adverse event reports per year · MAX
811in 2025
MAUDE reports naming product code MAX, 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 | 7 | 86 | 0 | 12 |
| 2008 | 35 | 88 | 2 | 19 |
| 2009 | 31 | 102 | 9 | 90 |
| 2010 | 29 | 137 | 0 | 154 |
| 2011 | 49 | 98 | 3 | 201 |
| 2012 | 48 | 69 | 11 (1) | 327 |
| 2013 | 58 | 102 | 0 | 380 |
| 2014 | 58 | 115 | 3 | 366 |
| 2015 | 53 | 113 | 1 | 524 |
| 2016 | 64 | 124 | 6 | 647 |
| 2017 | 76 | 116 | 1 | 596 |
| 2018 | 64 | 114 | 4 | 616 |
| 2019 | 60 | 131 | 1 | 699 |
| 2020 | 56 | 106 | 0 | 640 |
| 2021 | 53 | 109 | 0 | 622 |
| 2022 | 41 | 95 | 1 | 618 |
| 2023 | 30 | 87 | 0 | 576 |
| 2024 | 38 | 91 | 1 | 729 |
| 2025 | 29 | 85 | 5 | 811 |
| 2026 | 18 | 95 | 0 | — |
What is it indicated for?
Rampart A is an intervertebral body fusion device indicated for intervertebral body fusion at one level or two contiguous levels in the lumbar spine from L2 to S1 in patients with degenerative disc disease (DDD) with up to Grade I spondylolisthesis at the involved level(s). DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by patient history and radiographic studies. These patients should be skeletally mature and have had six months of non-operative treatment.
Rampart A is designed for use with autograft as an adjunct to fusion and is intended for use with supplemental fixation systems cleared by the FDA for use in the lumbar spine.
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/K153082 · printed Nov 6, 2026
Cite this page
510(k) Report. “K153082: Rampart A Lumbar Interbody 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/K153082
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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