510(k) Report

510(k) · Cleared

Cleared

Cervicore Corpectomy Cage

K091426510(k) TraditionalCleared Dec 23, 2009224-day reviewClass II21 CFR 888.3060

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

Verticor, Ltd. · MQP Spinal Vertebral Body Replacement Device

Cleared on Dec 23, 2009 after a 224-day review. The FDA summary names no predicate by number. 324 later devices descend from it.

Decided
Dec 23, 2009
Review
224 days
Class
Class II
Product code
MQP
Recalls
None
Predicates
0

324 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2012: 1 descendant cleared2015: 3 descendants cleared2013: 1 descendant cleared2017: 10 descendants cleared2020: 28 descendants cleared2019: 15 descendants cleared2016: 3 descendants cleared2014: 2 descendants cleared2018: 13 descendants cleared2026: 41 descendants cleared2021: 27 descendants cleared2023: 45 descendants cleared2022: 36 descendants cleared2024: 51 descendants cleared2025: 48 descendants cleared20052010201520202025
  1. This deviceK091426 Cervicore Corpectomy CageVerticor, Ltd. · 2009
  2. Descendant · cites it directly · 322 of its ownK120570 Choice Spine Vertebral Body Replacement (VBR) Device SystemChoicespine, LP · 2012
  3. Descendant · 2 generations on · 251 of its ownK130573 Tyber Medical Interbody System; Acif, Alif, Plif, Tlif, DlifTyber Medical, LLC · 2013
  4. Descendant · 3 generations on · 227 of its ownK133967 Interbody Cage SystemAurora Spine · 2014
  5. Descendant · 4 generations on · 210 of its ownK143578 SUSTAIN R TPS Spacers, PATRIOT TPS Spacers, CALIBER TPS Spacer…Globus Medical, Inc. · 2016
  6. Descendant · 5 generations on · 117 of its ownK161223 TransContinental® M Spacers and InterContinental® Plate-SpacersGlobus Medical, Inc. · 2016

Showing 5 of 324 descendants. See all descendants

Descendants cleared per year

2012: 12013: 12014: 22015: 32016: 32017: 102018: 132019: 152020: 282021: 272022: 362023: 452024: 512025: 482026: 41
2012high 51 (2024) · low 1 (2012)2026

Most influential descendants

Showing 5 of 324 · See all
  • K120570Choice Spine Vertebral Body Replacement (VBR) Device SystemChoicespine, LP · 2012 · cites it directly322descendants
  • K130573Tyber Medical Interbody System; Acif, Alif, Plif, Tlif, DlifTyber Medical, LLC · 2013 · 2 generations on251descendants
  • K133967Interbody Cage SystemAurora Spine · 2014 · 3 generations on227descendants
  • K143578SUSTAIN R TPS Spacers, PATRIOT TPS Spacers, CALIBER TPS Spacer, COALITION TPS Spacers…Globus Medical, Inc. · 2016 · 4 generations on210descendants
  • K161223TransContinental® M Spacers and InterContinental® Plate-SpacersGlobus Medical, Inc. · 2016 · 5 generations on117descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K091426Cervicore Corpectomy CageVerticor, Ltd.2009—
+1K120570Choice Spine Vertebral Body Replacement (VBR) Device SystemChoicespine, LP2012—
+2K130573Tyber Medical Interbody System; Acif, Alif, Plif, Tlif, DlifTyber Medical, LLC2013—
+3K133967Interbody Cage SystemAurora Spine2014—
+4K143578SUSTAIN R TPS Spacers, PATRIOT TPS Spacers, CALIBER TPS Spacer, COALITION TPS…Globus Medical, Inc.2016—
+5K161223TransContinental® M Spacers and InterContinental® Plate-SpacersGlobus Medical, Inc.2016—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201310
201420
201530
201630
2017100
2018130
2019150
2020280
2021270
2022360
2023450
2024510
2025480
2026410
FIG. 1 — Lineage of K091426, 2009–2026Source: 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 MQP? 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 MQP device

  1. #1 K261810 Vertiwedge® Intraosseous Systemscore 18.1 · 22 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against?

The FDA summary names no predicate by number.

What descends from it? (324)

See all 324

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K120570Choice Spine Vertebral Body Replacement (VBR) Device SystemChoicespine, LP2012322
K152460Rectangular Corpectomy CageAmendia, Inc.20150

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?

  • Of its descendants, K120570 (Choicespine, LP, 2012) has gone furthest, with 322 descendants of its own.

How does its category compare?

All MQP devices

MQP Spinal Vertebral Body Replacement Device: FDA decisions, review times, recalls and adverse event reports over 20 years. 2009, this device’s year, is highlighted.

FDA decisions per year · MQP

4in 2024

2007: 302008: 172009: 112010: 62011: 82012: 72013: 32014: 52015: 82017: 92018: 62019: 82020: 32022: 12023: 12024: 42026 (partial year): 3
2007high 30 (2007) · low 0 (2016)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · MQP

187in 2024

2007: 107 days median2008: 47 days median2009: 115 days median2010: 174 days median2011: 237 days median2012: 82 days median2013: 90 days median2014: 125 days median2015: 126 days median2017: 97 days median2018: 152 days median2019: 93 days median2020: 103 days median2024: 187 days median2026 (partial year): 102 days median
2007high 237 (2011) · low 47 (2008)2026

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

Recalls per year · MQP

1in 2022

2007: 22009: 142010: 22011: 12012: 22020: 152022: 1
2007high 15 (2020) · low 0 (2008)2026

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

Adverse event reports per year · MQP

168in 2025

2007: 612008: 762009: 1112010: 1662011: 1212012: 1412013: 2072014: 2162015: 2582016: 1292017: 1412018: 1302019: 1172020: 1572021: 2082022: 1372023: 712024: 982025: 168
2007high 258 (2015) · low 61 (2007)2025

MAUDE reports naming product code MQP, 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
200730107261
20081747076
20091111514111
201061742166
201182371121
20127822141
20133900207
201451250216
201581260258
20160—0129
20179970141
201861520130
20198930117
2020310315157
20210—0208
20221—1137
20231—071
20244187098
20250—0168
202631020—

What is it indicated for?

The Samson Corpectomny System is a vertebral body replacement system indicated for use to replace a vertebral body that has been resected or excised due to tumor or trauma/fracture. The device is intended for use as a vertebral body replacement in the thoracolumbar spine (from Ti to tS5). The Samson Corpectorny System is intended for use with supplemental fixation and isto be used with autograft and/or allograft.

Indications for use as stated in the FDA summary.

More from Verticor, Ltd.

3 FDA decisions under this applicant name. See the company

  • K110047Verticor K-Wire SystemVerticor, Ltd. · 2011
  • K103137Venus Anterior Cervical PlateVerticor, Ltd. · 2011

Recent decisions in MQP

The MQP category page

  • K261810Vertiwedge® Intraosseous SystemFoundation Surgical Group · 2026
  • K261031Poseidon STSignus Medinzintechnik GmbH · 2026
  • K253158VyBrate™ VBR SystemVy Spine, LLC · 2026
  • K241468Vertiwedge® Intraosseous SystemFoundation Surgical Group, Inc. · 2024
  • K232790KONG®-TL VBR System and KONG® C VBR SystemIcotec AG · 2024

https://510kreport.com/device/K091426 · printed Nov 6, 2026

Cite this page

510(k) Report. “K091426: Cervicore Corpectomy Cage.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K091426

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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