510(k) Report

510(k) · Cleared

Cleared

DELTA XTEND Reverse Shoulder System

K210167510(k) SpecialCleared Feb 19, 202129-day reviewClass II21 CFR 888.3660

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

DePuy Orthopaedics, Inc. · PHX Shoulder Prosthesis, Reverse Configuration

Cleared on Feb 19, 2021 as substantially equivalent to K062250 (DePuy Orthopaedics, Inc., 2007) and 3 other predicates after a 29-day review. Its family tree reaches back 13 generations to 1991. 1 of the 69 devices in its family, counting itself, has a Class I recall.

Decided
Feb 19, 2021
Review
29 days
Class
Class II
Product code
PHX
Recalls
None
Predicates
4

Its longest line of descent runs back 13 generations to K911686 (1991). 68 ancestors in all, the oldest K790987 (1979). No later device cites it as a predicate yet. 1 of the 69 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year cleared 2007: 4 other ancestors2008: 1 other ancestor2006: 4 other ancestors2000: 5 other ancestors2005: 6 other ancestors2004: 3 other ancestors2003: 3 other ancestors1999: 4 other ancestors1998: 3 other ancestors2001: 4 other ancestors1995: 2 other ancestors1992: 2 other ancestors1987: 3 other ancestors1980: 2 other ancestors1996: 4 other ancestors1994: 1 other ancestor1993: 1 other ancestor1989: 1 other ancestor1986: 1 other ancestor1979: 1 other ancestorK911686 · Global Total Shoulder, Uncement Humeral Hemi-Shoul · Depuy, Inc. · 1991K984541 · Global FX Humeral Stem, Global Advantage Humeral Head · DePuy Orthopaedics, Inc. · 1999K992065 · Global Advantage Shoulder, Global Advantage Humeral Stem, Global Advantage Eccentric Head · DePuy Orthopaedics, Inc. · 1999×3: 3 generations cleared close together, K021478 (2003), K030941 (2004), K041873 (2004) ×2: 2 generations cleared close together, K052906 (2005), K060704 (2006) K063569 · Equinoxe Reverse Shoulder System · Exactech, Inc. · 2007 · recalled×2: 2 generations cleared close together, K073688 (2008), K080642 (2008) K120174 · Deput Delta Xtend Reverse Shoulder · Depuy France · 2012 · recalledK192448 · Delta Xtend Revers Shoulder System · Depuy (Ireland) · 201919801990200020102020
Other ancestors, by generation 1 generation back: 2 other ancestors2 generations back: 3 other ancestors3 generations back: 15 other ancestors4 generations back: 14 other ancestors5 generations back: 13 other ancestors6 generations back: 8 other ancestors K192448 · Delta Xtend Revers Shoulder System · Depuy (Ireland) · 2019K120174 · Deput Delta Xtend Reverse Shoulder · Depuy France · 2012 · recalledK080642 · Comprehensive Reverse Shoulder · Biomet, Inc. · 2008 · Class I recallK073688 · Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and Locking Screw · Exactech, Inc. · 2008 · recalledK063569 · Equinoxe Reverse Shoulder System · Exactech, Inc. · 2007 · recalledK060704 · Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MM · Zimmer, Inc. · 2006 · recalledK052906 · Zimmer Trabecular Metal Reverse Shoulder System · Zimmer, Inc. · 2005 · recalledK041873 · Aequalis Reversed Shoulder Prosthesis · Tornier · 2004K030941 · Aequalis Reversed Shoulder Prosthesis · Tornier · 2004K021478 · Delta Shoulder · Depuy, Inc. · 2003K992065 · Global Advantage Shoulder, Global Advantage Humeral Stem, Global Advantage Eccentric Head · DePuy Orthopaedics, Inc. · 1999K984541 · Global FX Humeral Stem, Global Advantage Humeral Head · DePuy Orthopaedics, Inc. · 1999K911686 · Global Total Shoulder, Uncement Humeral Hemi-Shoul · Depuy, Inc. · 1991−10−50
  1. Root · 13 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
  2. 9 generations between
  3. 3 generations backK080642 Comprehensive Reverse ShoulderBiomet, Inc. · 2008 · Recalled (Class I)
  4. 2 generations backK120174 Deput Delta Xtend Reverse ShoulderDepuy France · 2012 · Recalled
  5. 1 generation backK192448 Delta Xtend Revers Shoulder SystemDepuy (Ireland) · 2019
  6. This deviceK210167 DELTA XTEND Reverse Shoulder SystemDePuy Orthopaedics, Inc. · 2021
Show all 13 generations
  1. Root · 13 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
  2. 12 generations backK984541 Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc. · 1999
  3. 11 generations backK992065 Global Advantage Shoulder, Global Advantage Humeral Stem, Global…DePuy Orthopaedics, Inc. · 1999
  4. 10 generations backK021478 Delta ShoulderDepuy, Inc. · 2003
  5. 9 generations backK030941 Aequalis Reversed Shoulder ProsthesisTornier · 2004
  6. 8 generations backK041873 Aequalis Reversed Shoulder ProsthesisTornier · 2004
  7. 7 generations backK052906 Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc. · 2005 · Recalled
  8. 6 generations backK060704 Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc. · 2006 · Recalled
  9. 5 generations backK063569 Equinoxe Reverse Shoulder SystemExactech, Inc. · 2007 · Recalled
  10. 4 generations backK073688 Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and…Exactech, Inc. · 2008 · Recalled
  11. 3 generations backK080642 Comprehensive Reverse ShoulderBiomet, Inc. · 2008 · Recalled (Class I)
  12. 2 generations backK120174 Deput Delta Xtend Reverse ShoulderDepuy France · 2012 · Recalled
  13. 1 generation backK192448 Delta Xtend Revers Shoulder SystemDepuy (Ireland) · 2019
  14. This deviceK210167 DELTA XTEND Reverse Shoulder SystemDePuy Orthopaedics, Inc. · 2021

Class I recalls in this family

  • K080642 Comprehensive Reverse Shoulder2 generations back · 2008
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−13K911686Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc.1991—
−12K984541Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc.1999—
−11K992065Global Advantage Shoulder, Global Advantage Humeral Stem, Global Advantage…DePuy Orthopaedics, Inc.1999—
−10K021478Delta ShoulderDepuy, Inc.2003—
−9K030941Aequalis Reversed Shoulder ProsthesisTornier2004—
−8K041873Aequalis Reversed Shoulder ProsthesisTornier2004—
−7K052906Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc.200512
−6K060704Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc.200610
−5K063569Equinoxe Reverse Shoulder SystemExactech, Inc.200713
−4K073688Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and Locking ScrewExactech, Inc.20081
−3K080642Comprehensive Reverse ShoulderBiomet, Inc.2008Class I
−2K120174Deput Delta Xtend Reverse ShoulderDepuy France20122
−1K192448Delta Xtend Revers Shoulder SystemDepuy (Ireland)2019—
0 (this device)K210167DELTA XTEND Reverse Shoulder SystemDePuy Orthopaedics, Inc.2021—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198020
198610
198730
198910
199220
199310
199410
199520
199640
199830
199940
200050
200140
200330
200430
200560
200640
200740
200810
FIG. 1 — Lineage of K210167, 1991–2021Source: 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.

1 device in this family has a Class I recall. 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 PHX device

  1. #1 K212737 INHANCE™ Reverse Shoulder Systemscore 28.4 · 15 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
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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
*K062250Delta Xtend Reverse Shoulder System
Summary page 5
…pedics Regulation 21 CFR 888.3690, 888.3660 Product Code(s) PHX, HSD, KWS Legally marketed DELTA XTEND™ Reverse Shoulder System (DePuy: K062250, device(s) to which K071379, K120174, K192448) equivalence is claimed Reason for 510(k) The purpose of this submis…
DePuy Orthopaedics, Inc.20078
*K071379Delta Xtend Reverse Shoulder Modular Stem
Summary page 5
…CFR 888.3690, 888.3660 Product Code(s) PHX, HSD, KWS Legally marketed DELTA XTEND™ Reverse Shoulder System (DePuy: K062250, device(s) to which K071379, K120174, K192448) equivalence is claimed Reason for 510(k) The purpose of this submission is to extend the current appro…
DePuy Orthopaedics, Inc.2007—
*K120174Deput Delta Xtend Reverse Shoulder
Summary page 5
…3690, 888.3660 Product Code(s) PHX, HSD, KWS Legally marketed DELTA XTEND™ Reverse Shoulder System (DePuy: K062250, device(s) to which K071379, K120174, K192448) equivalence is claimed Reason for 510(k) The purpose of this submission is to extend the current approved shelf…
Depuy France20122
*K192448Delta Xtend Revers Shoulder System
Summary page 5
….3660 Product Code(s) PHX, HSD, KWS Legally marketed DELTA XTEND™ Reverse Shoulder System (DePuy: K062250, device(s) to which K071379, K120174, K192448) equivalence is claimed Reason for 510(k) The purpose of this submission is to extend the current approved shelf life of…
Depuy (Ireland)2019—

Also cleared against K062250: 16 other devices →

What descends from it?

No later submission names this one as a predicate yet.

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K080642Comprehensive Reverse ShoulderBiomet, Inc. · 2008 · 2 generations back · ◆ on the line of descent in FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 30 years and passes through 8 companies; a new generation was cleared every 1.0 years on median.
  • 20 of the 68 ancestors have a recall of any class; 1 has a Class I recall.
  • 16 other devices also cite its predicate K062250.

How does its category compare?

All PHX devices

PHX Shoulder Prosthesis, Reverse Configuration: FDA decisions, review times, recalls and adverse event reports over 20 years. 2021, this device’s year, is highlighted.

FDA decisions per year · PHX

9in 2025

2007: 52008: 62009: 12010: 82011: 122012: 122013: 82014: 122015: 42016: 42017: 112018: 142019: 92020: 132021: 212022: 92023: 92024: 92025: 92026 (partial year): 18
2007high 21 (2021) · low 1 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · PHX

72in 2025

2007: 97 days median2008: 79 days median2010: 124 days median2011: 94 days median2012: 114 days median2013: 143 days median2014: 110 days median2015: 206 days median2016: 132 days median2017: 141 days median2018: 127 days median2019: 144 days median2020: 143 days median2021: 143 days median2022: 198 days median2023: 154 days median2024: 139 days median2025: 72 days median2026 (partial year): 130 days median
2007high 206 (2015) · low 72 (2025)2026

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

Recalls per year · PHX

3in 2025

2015: 22018: 12019: 32020: 32021: 82023: 72024: 12025: 32026 (partial year): 7
2007high 8 (2021) · low 0 (2007)2026

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

Adverse event reports per year · PHX

2,848in 2025

2015: 142016: 52017: 252018: 3232019: 5042020: 9862021: 1,4042022: 1,3422023: 1,4012024: 2,1422025: 2,848
2007high 2,848 (2025) · low 0 (2007)2025

MAUDE reports naming product code PHX, 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
200759700
200867900
20091—00
2010812400
2011129400
20121211400
2013814300
20141211000
20154206214
2016413205
201711141025
2018141271323
201991443504
2020131433986
20212114381,404
2022919801,342
2023915471,401
2024913912,142
202597232,848
2026181307—

What is it indicated for?

The DePuy DELTA XTEND™ Reverse Shoulder System is indicated for use in treatment of a grossly deficient rotator cuff joint with: -severe arthropathy and/or; -a previous failed joint replacement and/or: -fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternate methods of treatment are unsatisfactory The patient's joint must…

Read the full statement (145 words)

The DePuy DELTA XTEND™ Reverse Shoulder System is indicated for use in treatment of a grossly deficient rotator cuff joint with:

-severe arthropathy and/or;

-a previous failed joint replacement and/or:

-fracture-dislocations of the proximal humerus where the articular surface is severely comminuted, separated from its blood supply or where the surgeon's experience indicates that alternate methods of treatment are unsatisfactory

The patient's joint must be anatomically and structurally suited to receive the selected implant(s), and a functional deltoid muscle is necessary to use the device.

DELTA XTEND™ Reverse Shoulder System hemi-shoulder replacement is also indicated for hemi-arthroplasty if the glenoid is fractured intraoperatively or for the revision of a previously failed DELTA XTEND™ Reverse Shoulder System. The metaglene component is HA coated and is intended for cementless use with the addition of screws for fixation. All other metallic components are intended for cemented use only.

Indications for use as stated in the FDA summary.

Also cleared against K062250

16 other devices cite the same predicate.

  • K250338MSS - Humeral reverse liners extensionMedacta International S.A. · 2025
  • K192448Delta Xtend Revers Shoulder SystemDepuy (Ireland) · 2019
  • K183077Delta Xtend Reverse Shoulder SystemDepuy (Ireland) · 2019
  • K170452Medacta Shoulder SystemMedacta International S.A. · 2017
  • K130895Reunion Rsa Shoulder SystemHowmedica Osteonics Corp. · 2013
  • K130050Titan Reverse Shoulder SystemAscension Orthopedic · 2013

More from DePuy Orthopaedics, Inc.

361 FDA decisions under this applicant name. See the company

  • P070026/S129Ceramax Ceramic Hip SystemDePuy Orthopaedics, Inc. · 2026
  • P070026/S130CERAMAX Ceramic Hip SystemDePuy Orthopaedics, Inc. · 2026
  • P070026/S128CERAMAX® Ceramic Total Hip SystemDePuy Orthopaedics, Inc. · 2026
  • P070026/S127Ceramax Ceramic Hip SystemDePuy Orthopaedics, Inc. · 2026
  • K252887DePuy ATTUNE™ Knee SystemDePuy Orthopaedics, Inc. · 2026

Recent decisions in PHX

The PHX category page

  • K263421Veritas Shoulder Systemrestor3d, inc. · 2026
  • K263086AltiVate Reverse® Glenosphere with RAVN™ TechnologyEncore Medical L.P. · 2026
  • K260556Veritas Shoulder SystemRestor3D · 2026
  • K261683Augment Off-Axis Instrument SystemZimmer, Inc. · 2026
  • K260102Tornier Perform Reversed Glenoid and Tornier Perform Reversed Augmented Glenoid Shoulder SystemStryker Corporation (Tornier, Inc.) · 2026

https://510kreport.com/device/K210167 · printed Nov 6, 2026

Cite this page

510(k) Report. “K210167: DELTA XTEND Reverse Shoulder System.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K210167

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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