510(k) Report

510(k) · Cleared

Cleared

4CIS Vane Spine System

K101818510(k) TraditionalCleared Feb 11, 2011226-day reviewClass II21 CFR 888.3070

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

Solco Biomedical Co., Ltd. · MNH Orthosis, Spondylolisthesis Spinal Fixation

Cleared on Feb 11, 2011 as substantially equivalent to K031585 (U&I Corp., America, 2003) and 2 other predicates after a 226-day review. Its family tree reaches back 4 generations to 2000. 2 later devices descend from it.

Decided
Feb 11, 2011
Review
226 days
Class
Class II
Product code
MNH
Recalls
None
Predicates
3

Its longest line of descent runs back 4 generations to K000319 (2000). 9 ancestors in all. 2 later devices descend from it, 1 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2008: 1 other ancestor2000: 4 other ancestors2012: 1 descendant cleared2018: 1 descendant clearedK000319 · Ebi Xfix DFS System · Ebi, L.P. · 2000K020279 · Forex Corporation, Optima, Spinal System · Forex Corp. · 2002 · recalledK031585 · U&I, Optima, Spinal System · U&I Corp., America · 2003 · recalledK060702 · 4CIS Vane Spine System · Solco Biomedical Co., Ltd. · 2006200020052010201520202025
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 3 other ancestors3 generations back: 1 other ancestor 1 generation forward: 1 descendant2 generations forward: 1 descendant K060702 · 4CIS Vane Spine System · Solco Biomedical Co., Ltd. · 2006K031585 · U&I, Optima, Spinal System · U&I Corp., America · 2003 · recalledK020279 · Forex Corporation, Optima, Spinal System · Forex Corp. · 2002 · recalledK000319 · Ebi Xfix DFS System · Ebi, L.P. · 20000
  1. Root · 4 generations backK000319 Ebi Xfix DFS SystemEbi, L.P. · 2000
  2. 3 generations backK020279 Forex Corporation, Optima, Spinal SystemForex Corp. · 2002 · Recalled
  3. 2 generations backK031585 U&I, Optima, Spinal SystemU&I Corp., America · 2003 · Recalled
  4. 1 generation backK060702 4CIS Vane Spine SystemSolco Biomedical Co., Ltd. · 2006
  5. This deviceK101818 4CIS Vane Spine SystemSolco Biomedical Co., Ltd. · 2011
  6. Descendant · cites it directly · 1 of its ownK121615 4CIS Vane Spine SystemSolco Biomedical Co., Ltd. · 2012
  7. Descendant · 2 generations on · 0 of its ownK181995 Chiral Surgical Pedicle Screw SystemChiral Surgical · 2018

Most influential descendants

Showing 2 of 2 · See all
  • K1216154CIS Vane Spine SystemSolco Biomedical Co., Ltd. · 2012 · cites it directly1descendant
  • K181995Chiral Surgical Pedicle Screw SystemChiral Surgical · 2018 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K000319Ebi Xfix DFS SystemEbi, L.P.2000—
−3K020279Forex Corporation, Optima, Spinal SystemForex Corp.20024
−2K031585U&I, Optima, Spinal SystemU&I Corp., America20035
−1K0607024CIS Vane Spine SystemSolco Biomedical Co., Ltd.2006—
0 (this device)K1018184CIS Vane Spine SystemSolco Biomedical Co., Ltd.2011—
+1K1216154CIS Vane Spine SystemSolco Biomedical Co., Ltd.2012—
+2K181995Chiral Surgical Pedicle Screw SystemChiral Surgical2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
200040
200810

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201810
FIG. 1 — Lineage of K101818, 2000–2018Source: 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.

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  • Candidate predicates for a device like this, rankedin the report
  • Recall history across each candidate’s familyin 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
*K031585U&I, Optima, Spinal System
Summary page 1
…n testing were used to demonstrate the comparable mechanical & functional properties of the subject 4CIS VANE Spine System to the predicate devices (Optima K03 1585; 4CIS Vane Spine Systems cleared earlier under K060702 & K081 145) to support a determination of substantial equivalence.…
U&I Corp., America20035
*K0607024CIS Vane Spine System
Summary page 1
…functional properties of the subject 4CIS VANE Spine System to the predicate devices (Optima K03 1585; 4CIS Vane Spine Systems cleared earlier under K060702 & K081 145) to support a determination of substantial equivalence. Device Description The 4C15® VANE Spine System is a to…
Solco Biomedical Co., Ltd.2006—
*K081145Modification to 4CIS Vane Spine System
Summary page 1
…ctional properties of the subject 4CIS VANE Spine System to the predicate devices (Optima K03 1585; 4CIS Vane Spine Systems cleared earlier under K060702 & K081 145) to support a determination of substantial equivalence. Device Description The 4C15® VANE Spine System is a top-loading m…
Solco Biomedical Co., Ltd.2008—

Also cleared against K031585: 40 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K1216154CIS Vane Spine SystemSolco Biomedical Co., Ltd.20121

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 11 years and passes through 4 companies; a new generation was cleared every 3.0 years on median.
  • 2 of the 9 ancestors have a recall of any class.
  • Of its descendants, K121615 (Solco Biomedical Co., Ltd., 2012) has gone furthest, with 1 descendant of its own.
  • 40 other devices also cite its predicate K031585.

How does its category compare?

All MNH devices

MNH Orthosis, Spondylolisthesis Spinal Fixation: FDA decisions, review times, recalls and adverse event reports over 20 years. 2011, this device’s year, is highlighted.

FDA decisions per year · MNH

8in 2016

2007: 52008: 132009: 132010: 102011: 172012: 72013: 102014: 122015: 102016: 8
2007high 17 (2011) · low 0 (2017)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MNH

93in 2016

2007: 123 days median2008: 65 days median2009: 151 days median2010: 106 days median2011: 171 days median2012: 93 days median2013: 124 days median2014: 140 days median2015: 99 days median2016: 93 days median
2007high 171 (2011) · low 65 (2008)2026

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

Recalls per year · MNH

1in 2016

2009: 72012: 12013: 12016: 1
2007high 7 (2009) · low 0 (2007)2026

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

Adverse event reports per year · MNH

89in 2025

2007: 182008: 302009: 452010: 592011: 1072012: 4332013: 4642014: 2862015: 1522016: 2162017: 1742018: 1292019: 4032020: 4322021: 5312022: 2652023: 1212024: 3022025: 89
2007high 531 (2021) · low 18 (2007)2025

MAUDE reports naming product code MNH, 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
20075123018
20081365030
200913151745
201010106059
2011171710107
20127931433
2013101241464
2014121400286
201510990152
20168931216
20170—0174
20180—0129
20190—0403
20200—0432
20210—0531
20220—0265
20230—0121
20240—0302
20250—089
20260—0—

What is it indicated for?

The 4C15 VANE Spine System is a posterior non-cervical pedicle screw system intended for use as an adjunct to fusion in patients with degenerative spondylolisthesis (Grade 3 and 4) with objective evidence of neurological impairment, fracture, dislocation, scoliosis, kyphosis, spinal tumour, and failed previous fusion (pseudarthrosis) of the lumbosacral spine vertebra and implants are removable after the attainment of a solid fusion. These patients should be skeletally mature and have had at least six (6) months of non-operative treatment.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K101818: 4CIS Vane Spine System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K101818

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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