510(k) Report

510(k) · Cleared

Cleared

AdvantageRib Anterior System

K182179510(k) TraditionalCleared Nov 16, 201895-day reviewClass II21 CFR 888.3030

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

Sig Medical Corp. · HRS Plate, Fixation, Bone

Cleared on Nov 16, 2018 as substantially equivalent to K142823 (Biomet Microfixation, 2015) and 1 other predicate after a 95-day review. Its family tree reaches back 13 generations to 1976.

Decided
Nov 16, 2018
Review
95 days
Class
Class II
Product code
HRS
Recalls
None
Predicates
2

Its longest line of descent runs back 13 generations to K761228 (1976). 43 ancestors in all. No later device cites it as a predicate yet.

  1. Root · 13 generations backK761228 Luhr Mandibular Compression-Screw SystemHowmedica Corp. · 1976
  2. 9 generations between
  3. 3 generations backK121302 Biomet Microfixation Sternal Closure SystemBiomet Microfixation · 2012
  4. 2 generations backK142823 Biomet Microfixation Thoracic Fixation SystemBiomet Microfixation · 2015
  5. 1 generation backK151173 Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation · 2015
  6. This deviceK182179 AdvantageRib Anterior SystemSig Medical Corp. · 2018
Show all 13 generations
  1. Root · 13 generations backK761228 Luhr Mandibular Compression-Screw SystemHowmedica Corp. · 1976
  2. 12 generations backK963739 Leibinger - Luhr Small Orthopedic Bone ScrewsHowmedica Leibinger, Inc. · 1997
  3. 11 generations backK970912 Leibinger Self-Drilling ScrewHowmedica Leibinger, Inc. · 1997
  4. 10 generations backK974785 Auto-Drive Bone ScrewOsteomed Corp. · 1998
  5. 9 generations backK013954 Lorenz Self Drilling ScrewsWalter Lorenz Surgical, Inc. · 2002
  6. 8 generations backK032228 Lorenz 2.4 Self Drilling ScrewsWalter Lorenz Surgical, Inc. · 2003
  7. 7 generations backK033740 Lorenz Sternal Closure SystemWalter Lorenz Surgical, Inc. · 2003
  8. 6 generations backK063506 Lorenz Sternal Closure SystemWalter Lorenz Surgical, Inc. · 2006
  9. 5 generations backK110574 Biomet Microfixation Sternalock Blu Sternal Closure SystemBiomet Microfixation, Inc. · 2011 · Recalled
  10. 4 generations backK111908 Biomet Microfixation Sternal Closure SystemBiomet Microfixation, Inc. · 2011
  11. 3 generations backK121302 Biomet Microfixation Sternal Closure SystemBiomet Microfixation · 2012
  12. 2 generations backK142823 Biomet Microfixation Thoracic Fixation SystemBiomet Microfixation · 2015
  13. 1 generation backK151173 Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation · 2015
  14. This deviceK182179 AdvantageRib Anterior SystemSig Medical Corp. · 2018
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K761228Luhr Mandibular Compression-Screw SystemHowmedica Corp.1976—
−12K963739Leibinger - Luhr Small Orthopedic Bone ScrewsHowmedica Leibinger, Inc.1997—
−11K970912Leibinger Self-Drilling ScrewHowmedica Leibinger, Inc.1997—
−10K974785Auto-Drive Bone ScrewOsteomed Corp.1998—
−9K013954Lorenz Self Drilling ScrewsWalter Lorenz Surgical, Inc.2002—
−8K032228Lorenz 2.4 Self Drilling ScrewsWalter Lorenz Surgical, Inc.2003—
−7K033740Lorenz Sternal Closure SystemWalter Lorenz Surgical, Inc.2003—
−6K063506Lorenz Sternal Closure SystemWalter Lorenz Surgical, Inc.2006—
−5K110574Biomet Microfixation Sternalock Blu Sternal Closure SystemBiomet Microfixation, Inc.20111
−4K111908Biomet Microfixation Sternal Closure SystemBiomet Microfixation, Inc.2011—
−3K121302Biomet Microfixation Sternal Closure SystemBiomet Microfixation2012—
−2K142823Biomet Microfixation Thoracic Fixation SystemBiomet Microfixation2015—
−1K151173Biomet Microfixation RibFix Blu Thoracic Fixation SystemBiomet Microfixation2015—
0 (this device)K182179AdvantageRib Anterior SystemSig Medical Corp.2018—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198620
198810
199110
199440
199510
199630
199730
199820
200120
200310
200510
200620
200830
201010
201120
201410
FIG. 1 — Lineage of K182179, 1976–2018Source: 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.

Planning a device in HRS? 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 HRS device

  1. #1 K222465 Tyber Medical Anatomical Plating Systemscore 27.5 · 16 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? (2)

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
*K142823Biomet Microfixation Thoracic Fixation System
Summary page 4
…HRS, HWC Reviewing Panel: Orthopedic Primary Predicate Device: Zimmer-Biomet Microfixation RibFix Blue Thoracic Fixation System (K142823 and K151173) The primary predicate device has never been subject to a recall. Reference Predicate Devi…
Biomet Microfixation2015—
*K151173Biomet Microfixation RibFix Blu Thoracic Fixation System
Summary page 4
…Reviewing Panel: Orthopedic Primary Predicate Device: Zimmer-Biomet Microfixation RibFix Blue Thoracic Fixation System (K142823 and K151173) The primary predicate device has never been subject to a recall. Reference Predicate Device: Synthes…
Biomet Microfixation2015—
†K141241Matrixrib Endo Thoracoscopic Rib Plating SystemSynthes (USA) Products, LLC2014—

Also cleared against K142823: 3 other devices →

What descends from it?

No later submission names this one as a predicate yet.

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 42 years and passes through 7 companies; a new generation was cleared every 1.4 years on median.
  • 5 of the 43 ancestors have a recall of any class.
  • 3 other devices also cite its predicate K142823.

How does its category compare?

All HRS devices

HRS Plate, Fixation, Bone: FDA decisions, review times, recalls and adverse event reports over 20 years. 2018, this device’s year, is highlighted.

FDA decisions per year · HRS

54in 2025

2007: 352008: 352009: 472010: 492011: 432012: 592013: 562014: 762015: 562016: 442017: 572018: 402019: 462020: 482021: 402022: 472023: 402024: 542025: 542026 (partial year): 51
2007high 76 (2014) · low 35 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HRS

90in 2025

2007: 63 days median2008: 87 days median2009: 85 days median2010: 100 days median2011: 88 days median2012: 106 days median2013: 89 days median2014: 57 days median2015: 97 days median2016: 109 days median2017: 122 days median2018: 116 days median2019: 89 days median2020: 88 days median2021: 87 days median2022: 144 days median2023: 120 days median2024: 96 days median2025: 90 days median2026 (partial year): 82 days median
2007high 144 (2022) · low 57 (2014)2026

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

Recalls per year · HRS

1in 2025

2007: 22008: 112009: 32010: 162011: 52012: 42013: 112015: 72016: 52017: 32018: 22019: 252020: 12021: 92022: 32023: 12025: 12026 (partial year): 3
2007high 25 (2019) · low 0 (2014)2026

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

Adverse event reports per year · HRS

2,306in 2025

2007: 3392008: 3112009: 4352010: 4912011: 7732012: 1,6632013: 2,6432014: 2,4132015: 3,0952016: 2,2762017: 2,2202018: 2,6632019: 3,3592020: 2,7902021: 2,4422022: 1,7002023: 2,0492024: 1,8492025: 2,306
2007high 3,359 (2019) · low 311 (2008)2025

MAUDE reports naming product code HRS, 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
200735632339
2008358711311
200947853435
20104910016491
201143885773
20125910641,663
20135689112,643
2014765702,413
2015569773,095
20164410952,276
20175712232,220
20184011622,663
20194689253,359
2020488812,790
2021408792,442
20224714431,700
20234012012,049
2024549601,849
2025549012,306
202651823—

What is it indicated for?

The AdvantageRib Anterior System is intended for the fixation, stabilization, and fusion of rib fractures and osteotomies of normal and osteoporotic bone.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K182179: AdvantageRib Anterior System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K182179

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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