510(k) Report

510(k) · Cleared

Cleared

Trabecular Metal Vertebral Body Replacement (VBR), Model# 06-115, 06-155

K070754510(k) TraditionalCleared Aug 31, 2007165-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

Zimmer Trabecular Metal Technology · MQP Spinal Vertebral Body Replacement Device

Cleared on Aug 31, 2007 after a 165-day review. The FDA summary names no predicate by number. 506 later devices descend from it.

Decided
Aug 31, 2007
Review
165 days
Class
Class II
Product code
MQP
Recalls
None
Predicates
0

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

Descendants, by year cleared 2011: 3 descendants cleared2015: 2 descendants cleared2014: 3 descendants cleared2018: 28 descendants cleared2012: 1 descendant cleared2016: 7 descendants cleared2017: 21 descendants cleared2024: 76 descendants cleared2021: 47 descendants cleared2019: 33 descendants cleared2013: 1 descendant cleared2022: 52 descendants cleared2023: 72 descendants cleared2020: 53 descendants cleared2026: 50 descendants cleared2025: 57 descendants cleared20052010201520202025
  1. This deviceK070754 Trabecular Metal Vertebral Body Replacement (VBR), Model# 06-115…Zimmer Trabecular Metal Technology · 2007
  2. Descendant · cites it directly · 505 of its ownK103033 Trabecular Metal Fusion Device Model 06-101-Xxxxx, 06-102-Xxxxx and…Zimmer Trabecular Metal Technology · 2011
  3. Descendant · 2 generations on · 476 of its ownK113561 TM Ardis Interbody System TM Ardis Interbody System InstrumenationZimmer Trabecular Metal Technology · 2012 · Recalled
  4. Descendant · 3 generations on · 459 of its ownK150481 Cascadia Interbody SystemK2m, Inc. · 2015 · Recalled
  5. Descendant · 4 generations on · 315 of its ownK160125 Cascadia Interbody SystemK2m · 2016
  6. Descendant · 4 generations on · 276 of its ownK163230 NuVasive Modulus XLIF Interbody SystemNu Vasive, Incorporated · 2017

Showing 5 of 506 descendants. See all descendants

Descendants cleared per year

2011: 32012: 12013: 12014: 32015: 22016: 72017: 212018: 282019: 332020: 532021: 472022: 522023: 722024: 762025: 572026: 50
2011high 76 (2024) · low 1 (2012)2026

Most influential descendants

Showing 5 of 506 · See all
  • K103033Trabecular Metal Fusion Device Model 06-101-Xxxxx, 06-102-Xxxxx and 08-100-XxxxxZimmer Trabecular Metal Technology · 2011 · cites it directly505descendants
  • K113561TM Ardis Interbody System TM Ardis Interbody System InstrumenationZimmer Trabecular Metal Technology · 2012 · 2 generations on476descendants
  • K150481Cascadia Interbody SystemK2m, Inc. · 2015 · 3 generations on459descendants
  • K160125Cascadia Interbody SystemK2m · 2016 · 4 generations on315descendants
  • K163230NuVasive Modulus XLIF Interbody SystemNu Vasive, Incorporated · 2017 · 4 generations on276descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K070754Trabecular Metal Vertebral Body Replacement (VBR), Model# 06-115, 06-155Zimmer Trabecular Metal Technology2007—
+1K103033Trabecular Metal Fusion Device Model 06-101-Xxxxx, 06-102-Xxxxx and 08-100-XxxxxZimmer Trabecular Metal Technology2011—
+2K113561TM Ardis Interbody System TM Ardis Interbody System InstrumenationZimmer Trabecular Metal Technology20122
+3K150481Cascadia Interbody SystemK2m, Inc.20153
+4K160125Cascadia Interbody SystemK2m2016—
+4K163230NuVasive Modulus XLIF Interbody SystemNu Vasive, Incorporated2017—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201130
201210
201310
201430
201520
201670
2017210
2018280
2019330
2020530
2021470
2022520
2023720
2024760
2025570
2026500
FIG. 1 — Lineage of K070754, 2007–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

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? (506)

See all 506

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

NumberDeviceApplicantDecidedDescendants
K103033Trabecular Metal Fusion Device Model 06-101-Xxxxx, 06-102-Xxxxx and 08-100-XxxxxZimmer Trabecular Metal Technology2011505
K143297Ardis Interbody System, BAK Interbody Fusion System, BAK/C Anterior Cervical Interbody…Zimmer Spine, Inc.201519

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, K103033 (Zimmer Trabecular Metal Technology, 2011) has gone furthest, with 505 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. 2007, 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 Trabecular Metal Vertebral Body Replacement System is comprised of vertebral body replacement devices intended for use in the thoracolumbar spine (TI-L5) to replace a collapsed, damaged or unstable vertebral body due to tumor or trauma (i.e., fracture). The Trabecular Metal Vertebral Body Replacement is intended for use with supplemental internal spinal fixation systems. The Trabecular Metal Vertebral Body Replacement may be used with bone graft.

Indications for use as stated in the FDA summary.

More from Zimmer Trabecular Metal Technology

11 FDA decisions under this applicant name. See the company

  • K133784Vista-S Device, Associated InstrumentationZimmer Trabecular Metal Technology · 2014
  • K123602TM Ardis Interbody System InserterZimmer Trabecular Metal Technology · 2013
  • K120990Nexgen LCCK Trabecular Metal (TM) Coupled Tibial Cones Provisionals to Nexgen LCCK Trabecular Metal (TM)…Zimmer Trabecular Metal Technology · 20121 recall
  • K113561TM Ardis Interbody System TM Ardis Interbody System InstrumenationZimmer Trabecular Metal Technology · 20122 recalls
  • K111983Vista-S Device Model 08/06-401-Xxxxx, 08/06-402-XxxxxxZimmer Trabecular Metal Technology · 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/K070754 · printed Nov 6, 2026

Cite this page

510(k) Report. “K070754: Trabecular Metal Vertebral Body Replacement (VBR), Model# 06-115, 06-155.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070754

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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