510(k) Report

510(k) · Cleared

Cleared

Life Spine Sacroiliac Joint Fixation System

K141246510(k) TraditionalCleared Feb 22, 2015284-day reviewClass II21 CFR 888.3040

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

Life Spine, Inc. · OUR Sacroiliac Joint Fixation

Cleared on Feb 22, 2015 as substantially equivalent to K112028 (Globus Medical, Inc., 2011) after a 284-day review. Its family tree reaches back 6 generations to 1990. 29 later devices descend from it.

Decided
Feb 22, 2015
Review
284 days
Class
Class II
Product code
OUR
Recalls
None
Predicates
1

Its longest line of descent runs back 6 generations to K903810 (1990). 11 ancestors in all. 29 later devices descend from it, 7 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2002: 2 other ancestors1996: 1 other ancestor2000: 1 other ancestor2009: 1 other ancestor2024: 3 descendants cleared2018: 2 descendants cleared2021: 4 descendants cleared2026: 5 descendants cleared2016: 1 descendant cleared2020: 1 descendant cleared2023: 11 descendants cleared2022: 1 descendant cleared2025: 1 descendant clearedK903810 · Ace Cannulated Self Tapping Cancellous Bone Screw · Ace Medical Co. · 1990K051296 · Sijf Cannulated Screw System · Depuy Spine, Inc. · 2005×3: 3 generations cleared close together, K102907 (2010), K110512 (2011), K111801 (2011) K112028 · SI-Lok Sacroiliac Joint Fixation System · Globus Medical, Inc. · 20111990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors3 generations back: 2 other ancestors4 generations back: 1 other ancestor 1 generation forward: 7 descendants2 generations forward: 7 descendants3 generations forward: 5 descendants4 generations forward: 7 descendants5 generations forward: 3 descendants K112028 · SI-Lok Sacroiliac Joint Fixation System · Globus Medical, Inc. · 2011K111801 · Simmetry (TM) Sacroiliac Joint Fusion System · Zyga Technology, Inc. · 2011K110512 · Simmetry Sacroiliac Joint Fusion System · Zyga Technology, Inc. · 2011K102907 · Simmetry Sacroiliac Joint Fusion System · Zyga Technology, Inc. · 2010K051296 · Sijf Cannulated Screw System · Depuy Spine, Inc. · 2005K903810 · Ace Cannulated Self Tapping Cancellous Bone Screw · Ace Medical Co. · 1990−50+5
  1. Root · 6 generations backK903810 Ace Cannulated Self Tapping Cancellous Bone ScrewAce Medical Co. · 1990
  2. 5 generations backK051296 Sijf Cannulated Screw SystemDepuy Spine, Inc. · 2005
  3. 4 generations backK102907 Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc. · 2010
  4. 3 generations backK110512 Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc. · 2011
  5. 2 generations backK111801 Simmetry (TM) Sacroiliac Joint Fusion SystemZyga Technology, Inc. · 2011
  6. 1 generation backK112028 SI-Lok Sacroiliac Joint Fixation SystemGlobus Medical, Inc. · 2011
  7. This deviceK141246 Life Spine Sacroiliac Joint Fixation SystemLife Spine, Inc. · 2015
  8. Descendant · cites it directly · 14 of its ownK180749 Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc. · 2018
  9. Descendant · cites it directly · 13 of its ownK201538 Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc. · 2020
  10. Descendant · cites it directly · 13 of its ownK153656 PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd. · 2016
  11. Descendant · 2 generations on · 11 of its ownK181600 PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd. · 2018
  12. Descendant · 3 generations on · 10 of its ownK210035 ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical…Aegis Spine · 2021

Showing 5 of 29 descendants. See all descendants

Descendants cleared per year

2016: 12018: 22020: 12021: 42022: 12023: 112024: 32025: 12026: 5
2016high 11 (2023) · low 0 (2017)2026

Most influential descendants

Showing 5 of 29 · See all
  • K180749Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc. · 2018 · cites it directly14descendants
  • K201538Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc. · 2020 · cites it directly13descendants
  • K153656PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd. · 2016 · cites it directly13descendants
  • K181600PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd. · 2018 · 2 generations on11descendants
  • K210035ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System, MegaCerfix…Aegis Spine · 2021 · 3 generations on10descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K903810Ace Cannulated Self Tapping Cancellous Bone ScrewAce Medical Co.1990—
−5K051296Sijf Cannulated Screw SystemDepuy Spine, Inc.2005—
−4K102907Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc.2010—
−3K110512Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc.2011—
−2K111801Simmetry (TM) Sacroiliac Joint Fusion SystemZyga Technology, Inc.2011—
−1K112028SI-Lok Sacroiliac Joint Fixation SystemGlobus Medical, Inc.2011—
0 (this device)K141246Life Spine Sacroiliac Joint Fixation SystemLife Spine, Inc.2015—
+1K180749Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.2018—
+1K201538Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.2020—
+1K153656PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd.2016—
+2K181600PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd.2018—
+3K210035ZESPIN SI Joint Fusion System, MegaCerfix Posterior Cervical Fixation System…Aegis Spine2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
200010
200220
200910

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201610
201820
202010
202140
202210
2023110
202430
202510
202650
FIG. 1 — Lineage of K141246, 1990–2026Source: 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 OUR? 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 OUR device

  1. #1 K233508 iFuse Bedrock Granite® Implant Systemscore 30.7 · 31 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? (1)

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
*K112028SI-Lok Sacroiliac Joint Fixation System
Summary page 4
…HWC, CFR 888.3040, Class II OUR, CFR 888.3040, Class II Predicate Device: Globus SI-LOK Sacroiliac Joint Fixation System (K112028) Device Description: The Life Spine Sacroiliac Joint Fixation System consists of fully threaded screws and partially threade…
Globus Medical, Inc.2011—

Also cleared against K112028: 15 other devices →

What descends from it? (29)

See all 29

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

NumberDeviceApplicantDecidedDescendants
K180749Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.201814
K201538Life Spine SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.202013
K153656PathLoc-SI Joint Fusion SystemL&K BIOMED Co., Ltd.201613
K212903SIMPACT Sacroiliac Joint Fixation SystemLife Spine, Inc.20218
K241464ARx® SAI Implant SystemLife Spine, Inc.20241
K260571SIMPACT Sacroiliac Joint Fixation System GX Navigation InstrumentsLife Spine, Inc.20260
K254274ARx® SAI Implant SystemLife Spine, Inc.20260

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 25 years and passes through 5 companies; a new generation was cleared every 3.2 years on median.
  • 2 of the 11 ancestors have a recall of any class.
  • Of its descendants, K180749 (Life Spine, Inc., 2018) has gone furthest, with 14 descendants of its own.
  • 15 other devices also cite its predicate K112028.

How does its category compare?

All OUR devices

OUR Sacroiliac Joint Fixation: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · OUR

14in 2025

2008: 12009: 12010: 12011: 32012: 22013: 42014: 32015: 82016: 62017: 42018: 72019: 72020: 72021: 92022: 142023: 202024: 152025: 142026 (partial year): 6
2007high 20 (2023) · low 0 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · OUR

97in 2025

2011: 27 days median2013: 103 days median2014: 91 days median2015: 111 days median2016: 168 days median2017: 120 days median2018: 82 days median2019: 89 days median2020: 88 days median2021: 85 days median2022: 149 days median2023: 55 days median2024: 74 days median2025: 97 days median2026 (partial year): 98 days median
2007high 168 (2016) · low 27 (2011)2026

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

Recalls per year · OUR

1in 2025

2025: 12026 (partial year): 1
2007high 1 (2025) · low 0 (2007)2026

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

Adverse event reports per year · OUR

10in 2025

2011: 62012: 812013: 962014: 1462015: 1192016: 1222017: 1572018: 1372019: 1752020: 1482021: 1542022: 232023: 72024: 152025: 10
2007high 175 (2019) · low 0 (2007)2025

MAUDE reports naming product code OUR, 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
20070—00
20081—00
20091—00
20101—00
201132706
20122—081
20134103096
20143910146
201581110119
201661680122
201741200157
20187820137
20197890175
20207880148
20219850154
202214149023
2023205507
20241574015
20251497110
20266981—

What is it indicated for?

The Life Spine Sacroiliac Joint Fixation System is intended for sacroiliac joint fusion for conditions including sacroiliac joint disruptions and degenerative sacroiliitis.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K141246: Life Spine Sacroiliac Joint Fixation System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K141246

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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