510(k) Report

510(k) · Cleared

Cleared

Depuy Pinnacle Altrx Acetabular Liners

K072963510(k) TraditionalCleared Jan 9, 200882-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

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

Cleared on Jan 9, 2008 as substantially equivalent to K062148 (DePuy Orthopaedics, Inc., 2006) after an 82-day review. Its family tree reaches back 4 generations to 1993. 19 later devices descend from it.

Decided
Jan 9, 2008
Review
82 days
Class
Class II
Product code
LPH
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K930712 (1993). 10 ancestors in all. 19 later devices descend from it, 5 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2005: 1 other ancestor2004: 1 other ancestor1996: 1 other ancestor1995: 2 other ancestors1994: 1 other ancestor2019: 1 descendant cleared2025: 6 descendants cleared2010: 1 descendant cleared2016: 1 descendant cleared2024: 3 descendants cleared2014: 1 descendant cleared2023: 1 descendant cleared2022: 1 descendant cleared2026: 4 descendants clearedK930712 · P.F.C. Total Hip System Porous Coated Modular · Johnson & Johnson Orthopaedics, Inc. · 1993K983014 · Summit Acetabular System · Johnson & Johnson Professionals, Inc. · 1998K000306 · Pinnacle Acetabular System · DePuy Orthopaedics, Inc. · 2000 · recalledK062148 · Depuy Pinnacle Altrx Acetabular Cup Liner · DePuy Orthopaedics, Inc. · 20061990200020102020
Other ancestors, by generationDescendants, by generation 2 generations back: 2 other ancestors4 generations back: 4 other ancestors 1 generation forward: 5 descendants2 generations forward: 7 descendants3 generations forward: 6 descendants4 generations forward: 1 descendant K062148 · Depuy Pinnacle Altrx Acetabular Cup Liner · DePuy Orthopaedics, Inc. · 2006K000306 · Pinnacle Acetabular System · DePuy Orthopaedics, Inc. · 2000 · recalledK983014 · Summit Acetabular System · Johnson & Johnson Professionals, Inc. · 1998K930712 · P.F.C. Total Hip System Porous Coated Modular · Johnson & Johnson Orthopaedics, Inc. · 19930
  1. Root · 4 generations backK930712 P.F.C. Total Hip System Porous Coated ModularJohnson & Johnson Orthopaedics, Inc. · 1993
  2. 3 generations backK983014 Summit Acetabular SystemJohnson & Johnson Professionals, Inc. · 1998
  3. 2 generations backK000306 Pinnacle Acetabular SystemDePuy Orthopaedics, Inc. · 2000 · Recalled
  4. 1 generation backK062148 Depuy Pinnacle Altrx Acetabular Cup LinerDePuy Orthopaedics, Inc. · 2006
  5. This deviceK072963 Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc. · 2008
  6. Descendant · cites it directly · 17 of its ownK102423 Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc. · 2010 · Recalled
  7. Descendant · 2 generations on · 13 of its ownK132959 Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc. · 2014
  8. Descendant · 3 generations on · 7 of its ownK221636 EMPHASYS Acetabular SystemDepuy Ireland UC · 2022
  9. Descendant · cites it directly · 5 of its ownK231873 DePuy SUMMIT Porocoat Hip Prosthesis – MR Conditional, DePuy SUMMIT…Depuy Ireland UC · 2024
  10. Descendant · cites it directly · 4 of its ownK183582 MPACT ExtensionMedacta International S.A. · 2019

Showing 5 of 19 descendants. See all descendants

Descendants cleared per year

2010: 12014: 12016: 12019: 12022: 12023: 12024: 32025: 62026: 4
2010high 6 (2025) · low 0 (2011)2026

Most influential descendants

Showing 5 of 19 · See all
  • K102423Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc. · 2010 · cites it directly17descendants
  • K132959Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc. · 2014 · 2 generations on13descendants
  • K221636EMPHASYS Acetabular SystemDepuy Ireland UC · 2022 · 3 generations on7descendants
  • K231873DePuy SUMMIT Porocoat Hip Prosthesis – MR Conditional, DePuy SUMMIT DuoFix Hip…Depuy Ireland UC · 2024 · cites it directly5descendants
  • K183582MPACT ExtensionMedacta International S.A. · 2019 · cites it directly4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K930712P.F.C. Total Hip System Porous Coated ModularJohnson & Johnson Orthopaedics, Inc.1993—
−3K983014Summit Acetabular SystemJohnson & Johnson Professionals, Inc.1998—
−2K000306Pinnacle Acetabular SystemDePuy Orthopaedics, Inc.20001
−1K062148Depuy Pinnacle Altrx Acetabular Cup LinerDePuy Orthopaedics, Inc.2006—
0 (this device)K072963Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc.2008—
+1K102423Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc.20102
+2K132959Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc.2014—
+3K221636EMPHASYS Acetabular SystemDepuy Ireland UC2022—
+1K231873DePuy SUMMIT Porocoat Hip Prosthesis – MR Conditional, DePuy SUMMIT DuoFix Hip…Depuy Ireland UC2024—
+1K183582MPACT ExtensionMedacta International S.A.2019—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
199410
199520
199610
200410
200510

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201010
201410
201610
201910
202210
202310
202430
202560
202640
FIG. 1 — Lineage of K072963, 1993–2026Source: 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 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? (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
*K062148Depuy Pinnacle Altrx Acetabular Cup Liner
Summary page 1
…87 LPH, LZO SUBSTANTIALLY EQUIVALENT DePuy Pinnacle® AltrX~h Acetabular Liners, DEVICE: K062148, October 24, 2006 DEVICE DESCRIPTION: The Deputy Pinnacle AltrX Acetabular Liner is part of a modular system designed to repla…
DePuy Orthopaedics, Inc.2006—

Also cleared against K062148: 7 other devices →

What descends from it? (19)

See all 19

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

NumberDeviceApplicantDecidedDescendants
K102423Depuy Pinnacle Altrx Acetabular LinersDePuy Orthopaedics, Inc.201017
K231873DePuy SUMMIT Porocoat Hip Prosthesis – MR Conditional, DePuy SUMMIT DuoFix Hip…Depuy Ireland UC20245
K183582MPACT ExtensionMedacta International S.A.20194
K160895Initia Total Hip System & BIOCERAM AZUL (R) HEADKyocera Medical Corporation20162
K241059Pantheon Proximal Femur Reconstruction (PFR) SystemAdler Ortho S.P.A20250

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 15 years and passes through 3 companies; a new generation was cleared every 5.1 years on median.
  • 1 of the 10 ancestors has a recall of any class.
  • Of its descendants, K102423 (DePuy Orthopaedics, Inc., 2010) has gone furthest, with 17 descendants of its own.
  • 7 other devices also cite its predicate K062148.

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. 2008, 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 Pinnacle AltrX Acetabular Cup Liners are indicated for use in total hip replacement procedures. Total hip replacement is indicated in the following conditions: 1. A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia. 2. Avascular necrosis of the femoral head. 3. Acute traumatic fracture of the femoral head or neck. 4. Failed previous hip surgery, including joint…

Read the full statement (99 words)

The Pinnacle AltrX Acetabular Cup Liners are indicated for use in total hip replacement procedures.

Total hip replacement is indicated in the following conditions:

1. A severely painful and/or disabled joint from osteoarthritis, traumatic arthritis, rheumatoid arthritis, or congenital hip dysplasia.

2. Avascular necrosis of the femoral head.

3. Acute traumatic fracture of the femoral head or neck.

4. Failed previous hip surgery, including joint reconstruction, internal fixation, arthrodesis, hemiarthroplasty, surface replacement arthroplasty, or total hip replacement.

5. Certain cases of ankylosis

The Pinnacle AltrX Acetabular Cup Liners are indicated for use with Pinnacle Acetabular Cups in cementless applications.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K072963: Depuy Pinnacle Altrx Acetabular Liners.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K072963

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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