510(k) Report

510(k) · Cleared

Cleared

M.U.S.T. Sacral Illiac Screw and Pelvic Trauma System

K193083510(k) SpecialCleared Dec 3, 201928-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

Medacta International S.A. · OUR Sacroiliac Joint Fixation

Cleared on Dec 3, 2019 as substantially equivalent to K171595 (Medacta International S.A., 2017) after a 28-day review. Its family tree reaches back 7 generations to 1990. 21 later devices descend from it.

Decided
Dec 3, 2019
Review
28 days
Class
Class II
Product code
OUR
Recalls
None
Predicates
1

Its longest line of descent runs back 7 generations to K903810 (1990). 13 ancestors in all. 21 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2013: 1 other ancestor2002: 2 other ancestors2000: 1 other ancestor1996: 1 other ancestor2009: 1 other ancestor2021: 2 descendants cleared2022: 2 descendants cleared2024: 3 descendants cleared2026: 3 descendants cleared2023: 6 descendants cleared2025: 5 descendants 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. · 2011K171595 · M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System · Medacta International S.A. · 20171990200020102020
  1. Root · 7 generations backK903810 Ace Cannulated Self Tapping Cancellous Bone ScrewAce Medical Co. · 1990
  2. 6 generations backK051296 Sijf Cannulated Screw SystemDepuy Spine, Inc. · 2005
  3. 5 generations backK102907 Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc. · 2010
  4. 4 generations backK110512 Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc. · 2011
  5. 3 generations backK111801 Simmetry (TM) Sacroiliac Joint Fusion SystemZyga Technology, Inc. · 2011
  6. 2 generations backK112028 SI-Lok Sacroiliac Joint Fixation SystemGlobus Medical, Inc. · 2011
  7. 1 generation backK171595 M.U.S.T. Sacral Iliac Screw and Pelvic Trauma SystemMedacta International S.A. · 2017
  8. This deviceK193083 M.U.S.T. Sacral Illiac Screw and Pelvic Trauma SystemMedacta International S.A. · 2019
  9. Descendant · cites it directly · 17 of its ownK203247 iFuse-TORQ™ Implant SystemSI-BONE, Inc. · 2021 · Recalled
  10. Descendant · 2 generations on · 15 of its ownK213667 iFuse-TORQ® Implant SystemSI-BONE, Inc. · 2022
  11. Descendant · 2 generations on · 14 of its ownK222605 iFuse TORQ® Implant SystemSI-BONE, Inc. · 2022
  12. Descendant · 3 generations on · 5 of its ownK231689 iFuse TORQ® Implant SystemSI-BONE, Inc. · 2023
  13. Descendant · 3 generations on · 4 of its ownK241574 iFuse TORQ® Implant SystemSI-BONE, Inc. · 2024

Showing 5 of 21 descendants. See all descendants

Descendants cleared per year

2021: 22022: 22023: 62024: 32025: 52026: 3
2021high 6 (2023) · low 2 (2021)2026

Most influential descendants

Showing 5 of 21 · See all
  • K203247iFuse-TORQ™ Implant SystemSI-BONE, Inc. · 2021 · cites it directly17descendants
  • K213667iFuse-TORQ® Implant SystemSI-BONE, Inc. · 2022 · 2 generations on15descendants
  • K222605iFuse TORQ® Implant SystemSI-BONE, Inc. · 2022 · 2 generations on14descendants
  • K231689iFuse TORQ® Implant SystemSI-BONE, Inc. · 2023 · 3 generations on5descendants
  • K241574iFuse TORQ® Implant SystemSI-BONE, Inc. · 2024 · 3 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−7K903810Ace Cannulated Self Tapping Cancellous Bone ScrewAce Medical Co.1990—
−6K051296Sijf Cannulated Screw SystemDepuy Spine, Inc.2005—
−5K102907Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc.2010—
−4K110512Simmetry Sacroiliac Joint Fusion SystemZyga Technology, Inc.2011—
−3K111801Simmetry (TM) Sacroiliac Joint Fusion SystemZyga Technology, Inc.2011—
−2K112028SI-Lok Sacroiliac Joint Fixation SystemGlobus Medical, Inc.2011—
−1K171595M.U.S.T. Sacral Iliac Screw and Pelvic Trauma SystemMedacta International S.A.2017—
0 (this device)K193083M.U.S.T. Sacral Illiac Screw and Pelvic Trauma SystemMedacta International S.A.2019—
+1K203247iFuse-TORQ™ Implant SystemSI-BONE, Inc.20211
+2K213667iFuse-TORQ® Implant SystemSI-BONE, Inc.2022—
+2K222605iFuse TORQ® Implant SystemSI-BONE, Inc.2022—
+3K231689iFuse TORQ® Implant SystemSI-BONE, Inc.2023—
+3K241574iFuse TORQ® Implant SystemSI-BONE, Inc.2024—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199610
200010
200220
200910
201310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202120
202220
202360
202430
202550
202630
FIG. 1 — Lineage of K193083, 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
*K171595M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System
Summary page 4
…tion II III. Predicate Device Substantial equivalence is claimed to the following device: x M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System, K171595, Medacta International SA (Primary Predicate) IV. Device Description The M.U.S.T. Sacral Iliac Screw and Pelv…
Medacta International S.A.2017—

Also cleared against K171595: 4 other devices →

What descends from it? (21)

See all 21

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

NumberDeviceApplicantDecidedDescendants
K203247iFuse-TORQ™ Implant SystemSI-BONE, Inc.202117
K203671M.U.S.T. Sacral Iliac Screw and Pelvic Trauma SystemMedacta International S.A.20212

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 29 years and passes through 5 companies; a new generation was cleared every 2.3 years on median.
  • 2 of the 13 ancestors have a recall of any class.
  • Of its descendants, K203247 (SI-BONE, Inc., 2021) has gone furthest, with 17 descendants of its own.
  • 4 other devices also cite its predicate K171595.

How does its category compare?

All OUR devices

OUR Sacroiliac Joint Fixation: FDA decisions, review times, recalls and adverse event reports over 20 years. 2019, 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 M.U.S.T. Sacral Iliac Screw and Pelvic Trauma System is intended for use in skeletally mature patients for fracture fixation of small and long bones of the pelvis, and for sacroiliac joint fusion for patients suffering from sacroiliac joint disruptions and degenerative sacroiliitis.

Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.

Cite this page

510(k) Report. “K193083: M.U.S.T. Sacral Illiac Screw and Pelvic Trauma System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 5, 2026. https://510kreport.com/device/K193083

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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