510(k) Report

510(k) · Cleared

Cleared

Exactech Equinoxe Reverse Shoulder System+15MM Humeral Adapter Tray

K082702510(k) SpecialCleared Oct 10, 200824-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

Exactech, Inc. · PHX Shoulder Prosthesis, Reverse Configuration

Cleared on Oct 10, 2008 as substantially equivalent to K063569 (Exactech, Inc., 2007) after a 24-day review. Its family tree reaches back 9 generations to 1991. 4 later devices descend from it.

Decided
Oct 10, 2008
Review
24 days
Class
Class II
Product code
PHX
Recalls
None
Predicates
1

Its longest line of descent runs back 9 generations to K911686 (1991). 40 ancestors in all, the oldest K790987 (1979). 4 later devices descend from it, 2 citing it directly.

Other ancestors, by year clearedDescendants, by year cleared 2006: 2 other ancestors2005: 5 other ancestors2004: 1 other ancestor2003: 1 other ancestor2000: 1 other ancestor1999: 3 other ancestors1995: 2 other ancestors2001: 2 other ancestors1998: 2 other ancestors1980: 2 other ancestors1996: 4 other ancestors1993: 1 other ancestor1992: 1 other ancestor1989: 1 other ancestor1987: 1 other ancestor1986: 1 other ancestor1979: 1 other ancestor2019: 1 descendant cleared2023: 1 descendant cleared2026: 1 descendant cleared2025: 1 descendant clearedK911686 · Global Total Shoulder, Uncement Humeral Hemi-Shoul · Depuy, Inc. · 1991×2: 2 generations cleared close together, K984541 (1999), K992065 (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 · recalled19801990200020102020
  1. Root · 9 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
  2. 5 generations between
  3. 3 generations backK052906 Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc. · 2005 · Recalled
  4. 2 generations backK060704 Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc. · 2006 · Recalled
  5. 1 generation backK063569 Equinoxe Reverse Shoulder SystemExactech, Inc. · 2007 · Recalled
  6. This deviceK082702 Exactech Equinoxe Reverse Shoulder System+15MM Humeral Adapter TrayExactech, Inc. · 2008
  7. Descendant · cites it directly · 2 of its ownK223833 Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter TraysExactech, Inc. · 2023 · Recalled
  8. Descendant · 2 generations on · 0 of its ownK260583 Equinoxe® Shoulder SystemExactech, Inc. · 2026
  9. Descendant · 2 generations on · 0 of its ownK243448 Equinoxe® Shoulder SystemExactech, Inc. · 2025
  10. Descendant · cites it directly · 0 of its ownK191561 Exactech Equinoxe Humeral Augmented TraysExactech, Inc. · 2019 · Recalled
Show all 9 generations
  1. Root · 9 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
  2. 8 generations backK984541 Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc. · 1999
  3. 7 generations backK992065 Global Advantage Shoulder, Global Advantage Humeral Stem, Global…DePuy Orthopaedics, Inc. · 1999
  4. 6 generations backK021478 Delta ShoulderDepuy, Inc. · 2003
  5. 5 generations backK030941 Aequalis Reversed Shoulder ProsthesisTornier · 2004
  6. 4 generations backK041873 Aequalis Reversed Shoulder ProsthesisTornier · 2004
  7. 3 generations backK052906 Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc. · 2005 · Recalled
  8. 2 generations backK060704 Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc. · 2006 · Recalled
  9. 1 generation backK063569 Equinoxe Reverse Shoulder SystemExactech, Inc. · 2007 · Recalled
  10. This deviceK082702 Exactech Equinoxe Reverse Shoulder System+15MM Humeral Adapter TrayExactech, Inc. · 2008

Most influential descendants

Showing 4 of 4 · See all
  • K223833Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter TraysExactech, Inc. · 2023 · cites it directly2descendants
  • K260583Equinoxe® Shoulder SystemExactech, Inc. · 2026 · 2 generations on0descendants
  • K243448Equinoxe® Shoulder SystemExactech, Inc. · 2025 · 2 generations on0descendants
  • K191561Exactech Equinoxe Humeral Augmented TraysExactech, Inc. · 2019 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−9K911686Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc.1991—
−8K984541Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc.1999—
−7K992065Global Advantage Shoulder, Global Advantage Humeral Stem, Global Advantage…DePuy Orthopaedics, Inc.1999—
−6K021478Delta ShoulderDepuy, Inc.2003—
−5K030941Aequalis Reversed Shoulder ProsthesisTornier2004—
−4K041873Aequalis Reversed Shoulder ProsthesisTornier2004—
−3K052906Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc.200512
−2K060704Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc.200610
−1K063569Equinoxe Reverse Shoulder SystemExactech, Inc.200713
0 (this device)K082702Exactech Equinoxe Reverse Shoulder System+15MM Humeral Adapter TrayExactech, Inc.2008—
+1K223833Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter TraysExactech, Inc.20231
+2K260583Equinoxe® Shoulder SystemExactech, Inc.2026—
+2K243448Equinoxe® Shoulder SystemExactech, Inc.2025—
+1K191561Exactech Equinoxe Humeral Augmented TraysExactech, Inc.20191

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198020
198610
198710
198910
199210
199310
199520
199640
199820
199930
200010
200120
200310
200410
200550
200620

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201910
202310
202510
202610
FIG. 1 — Lineage of K082702, 1991–2026Source: 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 PHX? 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
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
*K063569Equinoxe Reverse Shoulder System
Summary page 4
…888.3660, Class 11, Product Code KWS) Information on devices to which Substantial equivalence is claimed: 510(k) Trade or Proprietary or Model Name Manufacturer Number K063569 Equinoxe® Reverse Shoulder System Exactech, Inc. Page 1 of 2 Exactech® Equinoxe® Reverse Shoulder System +15mm H…
Exactech, Inc.200713

Also cleared against K063569: 15 other devices →

What descends from it? (4)

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

NumberDeviceApplicantDecidedDescendants
K223833Exactech® Equinoxe® Reverse Humeral Liners and Humeral Adapter TraysExactech, Inc.20232
K191561Exactech Equinoxe Humeral Augmented TraysExactech, Inc.20190

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 17 years and passes through 5 companies; a new generation was cleared every 9 months on median.
  • 13 of the 40 ancestors have a recall of any class.
  • Of its descendants, K223833 (Exactech, Inc., 2023) has gone furthest, with 2 descendants of its own.
  • 15 other devices also cite its predicate K063569.

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. 2008, 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 Exactech® Equinoxe® Reverse Shoulder System is indicated to relieve pain and restore function in skeletally mature individuals with degenerative diseases of the glenohumeral joint and a grossly deficient, irreparable rotator cuff. The Equinoxe® Reverse Shoulder is also indicated for failed glenochumeral joint replacement with loss of rotator cuff function resulting in superior migration of the humeral head.

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. “K082702: Exactech Equinoxe Reverse Shoulder System+15MM Humeral Adapter Tray.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K082702

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