510(k) · Cleared
ClearedProLift Expandable System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Life Spine, Inc. · MAX Intervertebral Fusion Device With Bone Graft, Lumbar
Cleared on Mar 7, 2016 as substantially equivalent to K113527 (Interventional Spine, Inc., 2012) and 6 other predicates after a 104-day review. Its family tree reaches back 15 generations to 1984. 72 later devices descend from it.
- Decided
- Mar 7, 2016
- Review
- 104 days
- Class
- Class II
- Product code
- MAX
- Recalls
- None
- Predicates
- 7
Its longest line of descent runs back 15 generations to K841189 (1984). 74 ancestors in all. 72 later devices descend from it, 8 citing it directly.
- Root · 15 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
- 11 generations between
- 3 generations backK121683 Acculif TL CageCoalign Innovations, Inc. · 2012
- 2 generations backK123752 Acculif TL and PL CageCoalign Innovations, Inc. · 2013
- 1 generation backK133813 Flxfit Intervertebral Body Fusion DeviceExpanding Orthopedics, Inc. · 2014
- This deviceK153400 ProLift Expandable SystemLife Spine, Inc. · 2016
- Descendant · cites it directly · 37 of its ownK173182 ProLift® Expandable SystemLife Spine, Inc. · 2017
- Descendant · cites it directly · 29 of its ownK162918 Atlas Spine Expandable Interbody SystemAtlas Spine, Inc. · 2017
- Descendant · 2 generations on · 25 of its ownK172696 FORZA® XP Expandable Spacer SystemOrthofix, Inc. · 2018
- Descendant · 2 generations on · 18 of its ownK191005 ProLift® Expandable SystemLife Spine, Inc. · 2019
- Descendant · cites it directly · 16 of its ownK190488 ProLift Expandable SystemLife Spine, Inc. · 2019
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 backK073291 Capstone Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2008
- 5 generations backK094025 Crescent Spinal SystemMedtronic Sofamor Danek · 2010
- 4 generations backK110543 Crescent (R) Spinal System TitaniumMedtronic Sofamor Danek USA, Inc. · 2011
- 3 generations backK121683 Acculif TL CageCoalign Innovations, Inc. · 2012
- 2 generations backK123752 Acculif TL and PL CageCoalign Innovations, Inc. · 2013
- 1 generation backK133813 Flxfit Intervertebral Body Fusion DeviceExpanding Orthopedics, Inc. · 2014
- This deviceK153400 ProLift Expandable SystemLife Spine, Inc. · 2016
Showing 5 of 72 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 72 · See all- K173182ProLift® Expandable SystemLife Spine, Inc. · 2017 · cites it directly37descendants
- K162918Atlas Spine Expandable Interbody SystemAtlas Spine, Inc. · 2017 · cites it directly29descendants
- K172696FORZA® XP Expandable Spacer SystemOrthofix, Inc. · 2018 · 2 generations on25descendants
- K191005ProLift® Expandable SystemLife Spine, Inc. · 2019 · 2 generations on18descendants
- K190488ProLift Expandable SystemLife Spine, Inc. · 2019 · cites it directly16descendants
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 | K073291 | Capstone Spinal System | Medtronic Sofamor Danek USA, Inc. | 2008 | — |
| −5 | K094025 | Crescent Spinal System | Medtronic Sofamor Danek | 2010 | — |
| −4 | K110543 | Crescent (R) Spinal System Titanium | Medtronic Sofamor Danek USA, Inc. | 2011 | — |
| −3 | K121683 | Acculif TL Cage | Coalign Innovations, Inc. | 2012 | — |
| −2 | K123752 | Acculif TL and PL Cage | Coalign Innovations, Inc. | 2013 | — |
| −1 | K133813 | Flxfit Intervertebral Body Fusion Device | Expanding Orthopedics, Inc. | 2014 | — |
| 0 (this device) | K153400 | ProLift Expandable System | Life Spine, Inc. | 2016 | — |
| +1 | K173182 | ProLift® Expandable System | Life Spine, Inc. | 2017 | — |
| +1 | K162918 | Atlas Spine Expandable Interbody System | Atlas Spine, Inc. | 2017 | — |
| +2 | K172696 | FORZA® XP Expandable Spacer System | Orthofix, Inc. | 2018 | — |
| +2 | K191005 | ProLift® Expandable System | Life Spine, Inc. | 2019 | — |
| +1 | K190488 | ProLift Expandable System | Life Spine, Inc. | 2019 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 2 | 0 |
| 1999 | 2 | 0 |
| 2000 | 1 | 0 |
| 2001 | 9 | 0 |
| 2002 | 6 | 0 |
| 2003 | 8 | 0 |
| 2004 | 6 | 0 |
| 2005 | 3 | 0 |
| 2007 | 4 | 0 |
| 2008 | 4 | 0 |
| 2009 | 3 | 0 |
| 2010 | 3 | 0 |
| 2011 | 4 | 0 |
| 2012 | 2 | 0 |
| 2013 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2017 | 2 | 0 |
| 2018 | 6 | 0 |
| 2019 | 5 | 0 |
| 2020 | 6 | 0 |
| 2021 | 8 | 0 |
| 2022 | 8 | 0 |
| 2023 | 8 | 0 |
| 2024 | 6 | 0 |
| 2025 | 14 | 0 |
| 2026 | 9 | 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? (7)
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 |
|---|---|---|---|
| * | K113527 | Opticage Interbody Fusion DeviceSummary page 4…Intervertebral Body Fusion Device Classification: MAX, 21 CFR 888.3080, Class II Primary Predicate : Opticage Interbody Fusion Device (K113527) Additional Predicate: CoAlign Acculif Cages (K123752) Synthes T-PAL Spacer (K100089)… | 2012 |
| * | K123752 | Acculif TL and PL CageSummary page 4…MAX, 21 CFR 888.3080, Class II Primary Predicate : Opticage Interbody Fusion Device (K113527) Additional Predicate: CoAlign Acculif Cages (K123752) Synthes T-PAL Spacer (K100089) Custom Spine Pathway AVID (K090566)… | 2013 |
| * | K100089 | Synthes T-Pal SpacerSummary page 4…e : Opticage Interbody Fusion Device (K113527) Additional Predicate: CoAlign Acculif Cages (K123752) Synthes T-PAL Spacer (K100089) Custom Spine Pathway AVID (K090566) Kiscomedica L-Varlock (K080537)… | 2010 |
| * | K090566 | Pathway AvidSummary page 4…nal Predicate: CoAlign Acculif Cages (K123752) Synthes T-PAL Spacer (K100089) Custom Spine Pathway AVID (K090566) Kiscomedica L-Varlock (K080537) EOI FLXfit IBF (K133813)… | 2009 |
| * | K080537 | L-VarlockSummary page 4…Synthes T-PAL Spacer (K100089) Custom Spine Pathway AVID (K090566) Kiscomedica L-Varlock (K080537) EOI FLXfit IBF (K133813) The Globus Caliber (K123231) Device Descri… | 2008 |
| * | K133813 | Flxfit Intervertebral Body Fusion DeviceSummary page 4…Custom Spine Pathway AVID (K090566) Kiscomedica L-Varlock (K080537) EOI FLXfit IBF (K133813) The Globus Caliber (K123231) Device Description: The ProLift® Expandable System is available in… | 2014 |
| * | K123231 | Caliber SpacersSummary page 4…0566) Kiscomedica L-Varlock (K080537) EOI FLXfit IBF (K133813) The Globus Caliber (K123231) Device Description: The ProLift® Expandable System is available in a range of sizes and footprints and can expand to the des… | 2013 |
What descends from it? (72)
See all 728 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K173182 | ProLift® Expandable System | 2017 | 37 |
| K162918 | Atlas Spine Expandable Interbody System | 2017 | 29 |
| K190488 | ProLift Expandable System | 2019 | 16 |
| K223430 | ProLift Micro Expandable Spacer System | 2023 | 6 |
| K212520 | ProLift Micro Expandable Spacer System | 2021 | 6 |
| K180990 | TirboLOX-L Lumbar IBFD | 2018 | 1 |
| K172105 | The Plateau-LO Spacer System | 2018 | 1 |
| K182470 | Plateau Spacer System | 2018 | 0 |
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 32 years and passes through 12 companies; a new generation was cleared every 1.3 years on median.
- 7 of the 74 ancestors have a recall of any class.
- Of its descendants, K173182 (Life Spine, Inc., 2017) has gone furthest, with 37 descendants of its own.
- 7 other devices also cite its predicate K113527.
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?
The ProLift® Expandable System is intended for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels (L2-S1). DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. DDD patients may also have up to Grade 1 spondylolisthesis at the involved level(s). It is to be used in patients who have had at least six months of…
Read the full statement (126 words)
The ProLift® Expandable System is intended for spinal fusion procedures in skeletally mature patients with degenerative disc disease (DDD) at one or two contiguous levels (L2-S1). DDD is defined as back pain of discogenic origin with degeneration of the disc confirmed by history and radiographic studies. DDD patients may also have up to Grade 1 spondylolisthesis at the involved level(s). It is to be used in patients who have had at least six months of non-operative treatment. Patients with previous non-fusion spinal surgery at involved level(s) may be treated with the device. This device is intended to be used with autogenous bone graft and a supplemental internal spinal fixation system (e.g., pedicle screw or anterolateral plating system) that is cleared for use in the lumbosacral spine.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K153400 · printed Nov 6, 2026
Cite this page
510(k) Report. “K153400: ProLift Expandable System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K153400
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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