510(k) Report

510(k) · Cleared

Cleared

Cervical Spine Truss System - Stand Alone (CSTS-SA)

K253200510(k) TraditionalCleared Dec 11, 202576-day reviewClass II21 CFR 888.3080

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

4Web Medical, Inc. · OVE Intervertebral Fusion Device With Integrated Fixation, Cervical

Cleared on Dec 11, 2025 as substantially equivalent to K223362 (4Web Medical, Inc., 2023) and 2 other predicates after a 76-day review. Its family tree reaches back 25 generations to 1984.

Decided
Dec 11, 2025
Review
76 days
Class
Class II
Product code
OVE
Recalls
None
Predicates
3

Its longest line of descent runs back 25 generations to K841189 (1984). 433 ancestors in all, the oldest K792352 (1979). No later device cites it as a predicate yet.

Other ancestors, by year cleared 2023: 2 other ancestors2021: 1 other ancestor2019: 1 other ancestor2012: 17 other ancestors2017: 1 other ancestor2016: 4 other ancestors2015: 9 other ancestors2014: 13 other ancestors2013: 16 other ancestors2011: 25 other ancestors2010: 25 other ancestors2009: 32 other ancestors2008: 48 other ancestors2001: 17 other ancestors2007: 25 other ancestors2006: 19 other ancestors2004: 36 other ancestors2002: 17 other ancestors2000: 13 other ancestors1997: 9 other ancestors1993: 4 other ancestors2005: 23 other ancestors2003: 20 other ancestors1999: 7 other ancestors1998: 6 other ancestors1996: 7 other ancestors1995: 3 other ancestors1992: 4 other ancestors1988: 1 other ancestor1980: 1 other ancestor1979: 1 other ancestor1990: 1 other ancestorK841189 · Oec/Rezaian Spinal Fixator · Orthopedic Equipment Co., Inc. · 1984K990148 · Stackable Cage System · Depuy Motech Acromed · 1999K003043 · Surgical Titanium Mesh System · Depuyacromed · 2001×2: 2 generations cleared close together, K022793 (2003), K031757 (2003) ×2: 2 generations cleared close together, K041888 (2004), K042930 (2004) K062759 · Paramount VBR System · Innovative Spinal Technologies, Inc. · 2007K072120 · Paramount Intervertebral Body Fusion Device · Innovative Spinal Technologies, Inc. · 2007K073291 · Capstone Spinal System · Medtronic Sofamor Danek USA, Inc. · 2008K094025 · Crescent Spinal System · Medtronic Sofamor Danek · 2010K110543 · Crescent (R) Spinal System Titanium · Medtronic Sofamor Danek USA, Inc. · 2011×2: 2 generations cleared close together, K121683 (2012), K123752 (2013) K132505 · Acculif TL and PL Cage · Coalign Innovations, Inc. · 2013 · recalled×3: 3 generations cleared close together, K141217 (2014), K143163 (2015), K143616 (2015) K152304 · Tritanium PL Cage · Stryker · 2015 · recalled×2: 2 generations cleared close together, K160955 (2016), K162262 (2016) ×2: 2 generations cleared close together, K171496 (2017), K173159 (2018) K190870 · Cervical Spinal Truss System-Stand Alone (CSTS-SA) · 4Web, Inc. · 2019K223362 · Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device · 4Web Medical, Inc. · 202319801990200020102020
Other ancestors, by generation 1 generation back: 2 other ancestors2 generations back: 3 other ancestors3 generations back: 17 other ancestors4 generations back: 47 other ancestors5 generations back: 79 other ancestors6 generations back: 79 other ancestors7 generations back: 94 other ancestors8 generations back: 56 other ancestors9 generations back: 25 other ancestors10 generations back: 6 other ancestors K223362 · Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device · 4Web Medical, Inc. · 2023K190870 · Cervical Spinal Truss System-Stand Alone (CSTS-SA) · 4Web, Inc. · 2019K173159 · Cervical Spinal Truss System (CSTS) Interbody Fusion Device · 4Web, Inc. · 2018K171496 · Tritanium C Anterior Cervical Cage · Stryker Spine · 2017K162262 · Tritanium® PL Cage · Stryker · 2016K160955 · Tritanium® PL Cage · Stryker · 2016K152304 · Tritanium PL Cage · Stryker · 2015 · recalledK143616 · AccuLIF TL and PL Cage · Stryker Corporation · 2015 · recalledK143163 · AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK Spacer, AVS® Navigator PEEK Spacer, AVS® ARIA PEEK Spacer, AccuLIF TL and PL Cage, AVS® Anchor-L Spacer, Aero-AL Lumbar Cage System · Stryker Corporation · 2015K141217 · Acculif TL and PL Cage · Stryker Corporation · 2014 · recalledK132505 · Acculif TL and PL Cage · Coalign Innovations, Inc. · 2013 · recalledK123752 · Acculif TL and PL Cage · Coalign Innovations, Inc. · 2013K121683 · Acculif TL Cage · Coalign Innovations, Inc. · 2012K110543 · Crescent (R) Spinal System Titanium · Medtronic Sofamor Danek USA, Inc. · 2011K094025 · Crescent Spinal System · Medtronic Sofamor Danek · 2010K073291 · Capstone Spinal System · Medtronic Sofamor Danek USA, Inc. · 2008K072120 · Paramount Intervertebral Body Fusion Device · Innovative Spinal Technologies, Inc. · 2007K062759 · Paramount VBR System · Innovative Spinal Technologies, Inc. · 2007K042930 · Spacevision Cage System · Spine Vision, Inc. · 2004K041888 · Curved Peek Tetris Spinal Implant · Signus Medizintechnik GmbH · 2004K031757 · Peek Tetris Spinal Implant · Signus Medical, LLC · 2003K022793 · Tetris Spinal Implant · Signus Medical, LLC · 2003K003043 · Surgical Titanium Mesh System · Depuyacromed · 2001K990148 · Stackable Cage System · Depuy Motech Acromed · 1999K841189 · Oec/Rezaian Spinal Fixator · Orthopedic Equipment Co., Inc. · 1984−25−20−15−10−50
  1. Root · 25 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
  2. 21 generations between
  3. 3 generations backK173159 Cervical Spinal Truss System (CSTS) Interbody Fusion Device4Web, Inc. · 2018
  4. 2 generations backK190870 Cervical Spinal Truss System-Stand Alone (CSTS-SA)4Web, Inc. · 2019
  5. 1 generation backK223362 Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion…4Web Medical, Inc. · 2023
  6. This deviceK253200 Cervical Spine Truss System - Stand Alone (CSTS-SA)4Web Medical, Inc. · 2025
Show all 25 generations
  1. Root · 25 generations backK841189 Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc. · 1984
  2. 24 generations backK990148 Stackable Cage SystemDepuy Motech Acromed · 1999
  3. 23 generations backK003043 Surgical Titanium Mesh SystemDepuyacromed · 2001
  4. 22 generations backK022793 Tetris Spinal ImplantSignus Medical, LLC · 2003
  5. 21 generations backK031757 Peek Tetris Spinal ImplantSignus Medical, LLC · 2003
  6. 20 generations backK041888 Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH · 2004
  7. 19 generations backK042930 Spacevision Cage SystemSpine Vision, Inc. · 2004
  8. 18 generations backK062759 Paramount VBR SystemInnovative Spinal Technologies, Inc. · 2007
  9. 17 generations backK072120 Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc. · 2007
  10. 16 generations backK073291 Capstone Spinal SystemMedtronic Sofamor Danek USA, Inc. · 2008
  11. 15 generations backK094025 Crescent Spinal SystemMedtronic Sofamor Danek · 2010
  12. 14 generations backK110543 Crescent (R) Spinal System TitaniumMedtronic Sofamor Danek USA, Inc. · 2011
  13. 13 generations backK121683 Acculif TL CageCoalign Innovations, Inc. · 2012
  14. 12 generations backK123752 Acculif TL and PL CageCoalign Innovations, Inc. · 2013
  15. 11 generations backK132505 Acculif TL and PL CageCoalign Innovations, Inc. · 2013 · Recalled
  16. 10 generations backK141217 Acculif TL and PL CageStryker Corporation · 2014 · Recalled
  17. 9 generations backK143163 AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers…Stryker Corporation · 2015
  18. 8 generations backK143616 AccuLIF TL and PL CageStryker Corporation · 2015 · Recalled
  19. 7 generations backK152304 Tritanium PL CageStryker · 2015 · Recalled
  20. 6 generations backK160955 Tritanium® PL CageStryker · 2016
  21. 5 generations backK162262 Tritanium® PL CageStryker · 2016
  22. 4 generations backK171496 Tritanium C Anterior Cervical CageStryker Spine · 2017
  23. 3 generations backK173159 Cervical Spinal Truss System (CSTS) Interbody Fusion Device4Web, Inc. · 2018
  24. 2 generations backK190870 Cervical Spinal Truss System-Stand Alone (CSTS-SA)4Web, Inc. · 2019
  25. 1 generation backK223362 Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion…4Web Medical, Inc. · 2023
  26. This deviceK253200 Cervical Spine Truss System - Stand Alone (CSTS-SA)4Web Medical, Inc. · 2025
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−25K841189Oec/Rezaian Spinal FixatorOrthopedic Equipment Co., Inc.1984—
−24K990148Stackable Cage SystemDepuy Motech Acromed1999—
−23K003043Surgical Titanium Mesh SystemDepuyacromed2001—
−22K022793Tetris Spinal ImplantSignus Medical, LLC2003—
−21K031757Peek Tetris Spinal ImplantSignus Medical, LLC2003—
−20K041888Curved Peek Tetris Spinal ImplantSignus Medizintechnik GmbH2004—
−19K042930Spacevision Cage SystemSpine Vision, Inc.2004—
−18K062759Paramount VBR SystemInnovative Spinal Technologies, Inc.2007—
−17K072120Paramount Intervertebral Body Fusion DeviceInnovative Spinal Technologies, Inc.2007—
−16K073291Capstone Spinal SystemMedtronic Sofamor Danek USA, Inc.2008—
−15K094025Crescent Spinal SystemMedtronic Sofamor Danek2010—
−14K110543Crescent (R) Spinal System TitaniumMedtronic Sofamor Danek USA, Inc.2011—
−13K121683Acculif TL CageCoalign Innovations, Inc.2012—
−12K123752Acculif TL and PL CageCoalign Innovations, Inc.2013—
−11K132505Acculif TL and PL CageCoalign Innovations, Inc.20133
−10K141217Acculif TL and PL CageStryker Corporation20143
−9K143163AVS® AL and ALign PEEK Spacers, AVS® PL and UniLIF PEEK Spacers, AVS® TL PEEK…Stryker Corporation2015—
−8K143616AccuLIF TL and PL CageStryker Corporation20154
−7K152304Tritanium PL CageStryker20151
−6K160955Tritanium® PL CageStryker2016—
−5K162262Tritanium® PL CageStryker2016—
−4K171496Tritanium C Anterior Cervical CageStryker Spine2017—
−3K173159Cervical Spinal Truss System (CSTS) Interbody Fusion Device4Web, Inc.2018—
−2K190870Cervical Spinal Truss System-Stand Alone (CSTS-SA)4Web, Inc.2019—
−1K223362Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device4Web Medical, Inc.2023—
0 (this device)K253200Cervical Spine Truss System - Stand Alone (CSTS-SA)4Web Medical, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198010
198810
199010
199240
199340
199530
199670
199790
199860
199970
2000130
2001170
2002170
2003200
2004360
2005230
2006190
2007250
2008480
2009320
2010250
2011250
2012170
2013160
2014130
201590
201640
201710
201910
202110
202320
FIG. 1 — Lineage of K253200, 1984–2025Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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Notable FDA decisions, review times and new Class I recalls. See an issue.

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 OVE? 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 OVE device

  1. #1 K241846 E3D™-C Interbody Systemscore 32.1 · 32 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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.

TypeNumberDeviceApplicantDecidedRecalls
*K223362Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device
Summary page 6
…K253200 Predicate Device(s): The primary predicate device is the 4WEB Medical Cervical Spine Truss System – Stand Alone (K223362). Additional reference predicates are the 4WEB Medical Lateral Spine Truss System Plating Solution (K203065) and the 4WEB Medical…
4Web Medical, Inc.2023—
*K203065Lumbar Spine Truss System Plating Solution (LSTS-PS)
Summary page 6
…s the 4WEB Medical Cervical Spine Truss System – Stand Alone (K223362). Additional reference predicates are the 4WEB Medical Lateral Spine Truss System Plating Solution (K203065) and the 4WEB Medical Cervical Spine Truss System (K231739). Performance Standards: Performance testing has been completed per t…
4Web, Inc.2021—
*K231739Cervical Spine Truss System (CSTS)
Summary page 6
…e (K223362). Additional reference predicates are the 4WEB Medical Lateral Spine Truss System Plating Solution (K203065) and the 4WEB Medical Cervical Spine Truss System (K231739). Performance Standards: Performance testing has been completed per the following standards: • ASTM F2077 – Static Axial…
4Web Medical, Inc.2023—

Also cleared against K223362: 1 other device →

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 41 years and passes through 15 companies; a new generation was cleared every 10 months on median.
  • 48 of the 433 ancestors have a recall of any class.
  • 1 other device also cites its predicate K223362.

How does its category compare?

All OVE devices

OVE Intervertebral Fusion Device With Integrated Fixation, Cervical: FDA decisions, review times, recalls and adverse event reports over 20 years. 2025, this device’s year, is highlighted.

FDA decisions per year · OVE

10in 2025

2007: 12008: 42009: 12010: 42011: 82012: 72013: 52014: 112015: 122016: 152017: 92018: 72019: 72020: 132021: 102022: 102023: 162024: 62025: 102026 (partial year): 13
2007high 16 (2023) · low 1 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OVE

105in 2025

2008: 131 days median2010: 210 days median2011: 139 days median2012: 125 days median2013: 71 days median2014: 168 days median2015: 113 days median2016: 149 days median2017: 100 days median2018: 105 days median2019: 87 days median2020: 149 days median2021: 93 days median2022: 144 days median2023: 97 days median2024: 56 days median2025: 105 days median2026 (partial year): 66 days median
2007high 210 (2010) · low 56 (2024)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · OVE

2in 2021

2013: 12014: 12015: 12016: 12017: 12021: 2
2007high 2 (2021) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · OVE

132in 2025

2010: 22011: 192012: 592013: 2502014: 1502015: 1732016: 1452017: 1342018: 2102019: 1692020: 1622021: 1862022: 2002023: 1482024: 1422025: 132
2007high 250 (2013) · low 0 (2007)2025

MAUDE reports naming product code OVE, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20071—00
2008413100
20091—00
2010421002
20118139019
20127125059
20135711250
2014111681150
2015121131173
2016151491145
201791001134
201871050210
20197870169
2020131490162
202110932186
2022101440200
202316970148
20246560142
2025101050132
202613660—

What is it indicated for?

The Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device is indicated for use in skeletally mature patients with Degenerative Disc Disease (DDD) of the cervical spine at one level or two contiguous disc levels and is to be used with two titanium alloy screws or fixation anchors which accompany the device. DDD is defined as discogenic back pain with degeneration of the disc confirmed by patient history and radiographic studies.…

Read the full statement (146 words)

The Cervical Spine Truss System - Stand Alone (CSTS-SA) Interbody Fusion Device is indicated for use in skeletally mature patients with Degenerative Disc Disease (DDD) of the cervical spine at one level or two contiguous disc levels and is to be used with two titanium alloy screws or fixation anchors which accompany the device. DDD is defined as discogenic back pain with degeneration of the disc confirmed by patient history and radiographic studies. CSTS-SA Interbody Fusion Devices are used as an adjunct to fusion in the cervical spine and are placed via an anterior approach at the C2 to T1 disc levels using autograft and/or allogenic bone graft comprised of cancellous and/or corticocancellous bone graft. Patients should have received 6 weeks of non-operative treatment prior to treatment with the devices. When using the CSTS-SA interbody with fixation anchors, the device must be used with supplemental fixation.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K253200: Cervical Spine Truss System - Stand Alone (CSTS-SA).” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K253200

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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