510(k) Report

510(k) · Cleared

Cleared

Continuum and Trilogy Integrated Taper (IT) Acetabular Systems

K151448510(k) TraditionalCleared Aug 13, 201576-day reviewClass II21 CFR 888.3358

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

Zimmer, Inc. · LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented

Cleared on Aug 13, 2015 as substantially equivalent to K091508 (Zimmer, Inc., 2009) and 3 other predicates after a 76-day review. Its family tree reaches back 6 generations to 1994. 6 later devices descend from it.

Decided
Aug 13, 2015
Review
76 days
Class
Class II
Product code
LPH
Recalls
None
Predicates
4

Its longest line of descent runs back 6 generations to K934765 (1994). 13 ancestors in all. 6 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2001: 2 other ancestors2000: 2 other ancestors1999: 1 other ancestor1996: 1 other ancestor1995: 1 other ancestor2019: 2 descendants cleared2026: 2 descendants cleared2025: 2 descendants clearedK934765 · Trilogy Acetabular System · Zimmer, Inc. · 1994 · recalledK021891 · Zimmer Trabecular Metal Modular Acetabular System · Zimmer, Inc. · 2002 · recalledK091508 · Zimmer Continuum Acetabular System, Zimmer Trilogy IT Acetabular System · Zimmer, Inc. · 2009 · recalledK093846 · Longevity IT Highly Crosslinked Polyethylene Elevated Liners · Zimmer, Inc. · 2010×2: 2 generations cleared close together, K101229 (2010), K103662 (2011) 1990200020102020
  1. Root · 6 generations backK934765 Trilogy Acetabular SystemZimmer, Inc. · 1994 · Recalled
  2. 5 generations backK021891 Zimmer Trabecular Metal Modular Acetabular SystemZimmer, Inc. · 2002 · Recalled
  3. 4 generations backK091508 Zimmer Continuum Acetabular System, Zimmer Trilogy IT Acetabular…Zimmer, Inc. · 2009 · Recalled
  4. 3 generations backK093846 Longevity IT Highly Crosslinked Polyethylene Elevated LinersZimmer, Inc. · 2010
  5. 2 generations backK101229 Longevity IT Highly Crosslinked Polyethylene Elevated Liners…Zimmer, Inc. · 2010
  6. 1 generation backK103662 Continuum and Trilogy Integrated Taper (IT) Acetabular Systems…Zimmer, Inc. · 2011
  7. This deviceK151448 Continuum and Trilogy Integrated Taper (IT) Acetabular SystemsZimmer, Inc. · 2015
  8. Descendant · cites it directly · 4 of its ownK190660 G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7…Zimmer, Inc. · 2019
  9. Descendant · cites it directly · 1 of its ownK190656 Dual Mobility - Longevity and Vivacit-E Polyethylene Hip BearingsZimmer, Inc. · 2019 · Recalled
  10. Descendant · 2 generations on · 0 of its ownK261453 G7® Acetabular SystemZimmer Biomet · 2026
  11. Descendant · 2 generations on · 0 of its ownK253948 Momentum Acetabular Cup SystemUnited Orthopedic Corporation · 2026
  12. Descendant · 2 generations on · 0 of its ownK252067 Velora Acetabular SystemRestor3D, Inc. · 2025

Showing 5 of 6 descendants. See all descendants

Descendants cleared per year

2019: 22025: 22026: 2
2019high 2 (2019) · low 0 (2020)2026

Most influential descendants

Showing 5 of 6 · See all
  • K190660G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7 Acetabular System…Zimmer, Inc. · 2019 · cites it directly4descendants
  • K190656Dual Mobility - Longevity and Vivacit-E Polyethylene Hip BearingsZimmer, Inc. · 2019 · cites it directly1descendant
  • K261453G7® Acetabular SystemZimmer Biomet · 2026 · 2 generations on0descendants
  • K253948Momentum Acetabular Cup SystemUnited Orthopedic Corporation · 2026 · 2 generations on0descendants
  • K252067Velora Acetabular SystemRestor3D, Inc. · 2025 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K934765Trilogy Acetabular SystemZimmer, Inc.199416
−5K021891Zimmer Trabecular Metal Modular Acetabular SystemZimmer, Inc.20023
−4K091508Zimmer Continuum Acetabular System, Zimmer Trilogy IT Acetabular SystemZimmer, Inc.20093
−3K093846Longevity IT Highly Crosslinked Polyethylene Elevated LinersZimmer, Inc.2010—
−2K101229Longevity IT Highly Crosslinked Polyethylene Elevated Liners, Continuum…Zimmer, Inc.2010—
−1K103662Continuum and Trilogy Integrated Taper (IT) Acetabular Systems; Longevity IT…Zimmer, Inc.2011—
0 (this device)K151448Continuum and Trilogy Integrated Taper (IT) Acetabular SystemsZimmer, Inc.2015—
+1K190660G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7 Acetabular…Zimmer, Inc.2019—
+1K190656Dual Mobility - Longevity and Vivacit-E Polyethylene Hip BearingsZimmer, Inc.20193
+2K261453G7® Acetabular SystemZimmer Biomet2026—
+2K253948Momentum Acetabular Cup SystemUnited Orthopedic Corporation2026—
+2K252067Velora Acetabular SystemRestor3D, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199510
199610
199910
200020
200120

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201920
202520
202620
FIG. 1 — Lineage of K151448, 1994–2026Source: 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 LPH? 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 LPH device

  1. #1 K233498 Stryker Orthopaedics Hip Systems Labeling Updatescore 24.2 · 20 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? (4)

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
*K091508Zimmer Continuum Acetabular System, Zimmer Trilogy IT Acetabular System
Summary page 4
…Continuum and Trilogy Integrated Taper (IT) Acetabular Systems, manufactured by Zimmer, K091508, cleared September 11, 2009 Longevity IT Highly Crosslinked Polyethylene…
Zimmer, Inc.20093
*K093846Longevity IT Highly Crosslinked Polyethylene Elevated Liners
Summary page 4
…Longevity IT Highly Crosslinked Polyethylene Elevated Liners, manufactured by Zimmer, K093846, cleared February 4, 2010 K151448 (page 2/3)…
Zimmer, Inc.2010—
*K101229Longevity IT Highly Crosslinked Polyethylene Elevated Liners, Continuum Acetabular…
Summary page 5
…Liners, Continuum and Trilogy Integrated Taper (IT) Acetabular System Shells, manufactured by Zimmer, K101229, cleared December 3, 2010 Continuum and Trilogy Integrated T…
Zimmer, Inc.2010—
*K103662Continuum and Trilogy Integrated Taper (IT) Acetabular Systems; Longevity IT Highly…
Summary page 5
…Crosslinked Polyethylene Elevated, Offset, & Oblique Liners, manufactured by Zimmer, K103662, cleared April 15, 2011 Device Description: The Continuum and Trilogy IT Acetabular Systems…
Zimmer, Inc.2011—

Also cleared against K091508: 17 other devices →

What descends from it? (6)

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

NumberDeviceApplicantDecidedDescendants
K190660G7 Acetabular System Longevity Highly Crosslinked Polyethylene, G7 Acetabular System…Zimmer, Inc.20194
K190656Dual Mobility - Longevity and Vivacit-E Polyethylene Hip BearingsZimmer, Inc.20191

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 21 years and passes through 1 company; a new generation was cleared every 4.3 years on median.
  • 5 of the 13 ancestors have a recall of any class.
  • Of its descendants, K190660 (Zimmer, Inc., 2019) has gone furthest, with 4 descendants of its own.
  • 17 other devices also cite its predicate K091508.

How does its category compare?

All LPH devices

LPH Prosthesis, Hip, Semi-Constrained, Metal/Polymer, Porous Uncemented: FDA decisions, review times, recalls and adverse event reports over 20 years. 2015, this device’s year, is highlighted.

FDA decisions per year · LPH

12in 2025

2007: 102008: 102009: 32010: 152011: 162012: 252013: 112014: 202015: 182016: 102017: 122018: 92019: 222020: 72021: 82022: 142023: 102024: 62025: 122026 (partial year): 8
2007high 25 (2012) · low 3 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · LPH

153in 2025

2007: 116 days median2008: 86 days median2009: 112 days median2010: 100 days median2011: 110 days median2012: 76 days median2013: 135 days median2014: 129 days median2015: 111 days median2016: 150 days median2017: 121 days median2018: 145 days median2019: 164 days median2020: 164 days median2021: 410 days median2022: 247 days median2023: 111 days median2024: 92 days median2025: 153 days median2026 (partial year): 256 days median
2007high 410 (2021) · low 76 (2012)2026

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

Recalls per year · LPH

4in 2025

2007: 162008: 12009: 22010: 222011: 262012: 302013: 92014: 32015: 12016: 82017: 142018: 22019: 82020: 62021: 42022: 22023: 22024: 12025: 42026 (partial year): 2
2007high 30 (2012) · low 1 (2008)2026

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

Adverse event reports per year · LPH

6,163in 2025

2007: 5092008: 7062009: 1,1562010: 2,0072011: 3,3202012: 3,7852013: 5,0022014: 5,1632015: 5,8302016: 4,9002017: 5,3122018: 5,9542019: 7,1302020: 5,4292021: 5,9782022: 5,2232023: 5,3452024: 5,6262025: 6,163
2007high 7,130 (2019) · low 509 (2007)2025

MAUDE reports naming product code LPH, 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
20071011616509
200810861706
2009311221,156
201015100222,007
201116110263,320
20122576303,785
20131113595,002
20142012935,163
20151811115,830
20161015084,900
201712121145,312
2018914525,954
20192216487,130
2020716465,429
2021841045,978
20221424725,223
20231011125,345
202469215,626
20251215346,163
202682562—

What is it indicated for?

The system is indicated for primary or revision surgery in skeletally mature individuals for rehabilitating hips damaged as a result of noninflammatory degenerative joint disease (NIDJD) or its composite diagnoses of osteoarthritis, avascular necrosis, protrusio acetabuli, traumatic arthritis, slipped capital epiphysis, fused hip, fracture of the pelvis, and diastrophic variant.

The system is intended for use either with or without bone cement in total hip arthroplasty.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K151448: Continuum and Trilogy Integrated Taper (IT) Acetabular Systems.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K151448

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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