510(k) · Cleared
ClearedAequalis Reversed Shoulder Prosthesis
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Tornier · PHX Shoulder Prosthesis, Reverse Configuration
Cleared on Mar 16, 2005 as substantially equivalent to K030941 (Tornier, 2004) and 4 other predicates after a 35-day review. Its family tree reaches back 6 generations to 1991. 1 of the 262 devices in its family, counting itself, has a Class I recall. 248 later devices descend from it.
- Decided
- Mar 16, 2005
- Review
- 35 days
- Class
- Class II
- Product code
- PHX
- Recalls
- None
- Predicates
- 5
Its longest line of descent runs back 6 generations to K911686 (1991). 13 ancestors in all, the oldest K800494 (1980). 248 later devices descend from it, 9 citing it directly. 1 of the 262 devices in this family, counting this one, has a Class I recall.
- Root · 6 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
- 5 generations backK984541 Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc. · 1999
- 4 generations backK992065 Global Advantage Shoulder, Global Advantage Humeral Stem, Global…DePuy Orthopaedics, Inc. · 1999
- 3 generations backK021478 Delta ShoulderDepuy, Inc. · 2003
- 2 generations backK030941 Aequalis Reversed Shoulder ProsthesisTornier · 2004
- 1 generation backK041873 Aequalis Reversed Shoulder ProsthesisTornier · 2004
- This deviceK050316 Aequalis Reversed Shoulder ProsthesisTornier · 2005
- Descendant · cites it directly · 199 of its ownK061439 Aequalis Reversed ProsthesisTornier · 2006
- Descendant · cites it directly · 190 of its ownK063569 Equinoxe Reverse Shoulder SystemExactech, Inc. · 2007 · Recalled
- Descendant · cites it directly · 179 of its ownK081059 Aequalis Reversed Shoulder ProsthesisTornier · 2008
- Descendant · cites it directly · 178 of its ownK071948 Aequalis Reversed AdapterTornier · 2007
- Descendant · 2 generations on · 177 of its ownK073688 Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and…Exactech, Inc. · 2008 · Recalled
Showing 5 of 248 descendants. See all descendants
Descendants cleared per year
Class I recalls in this family
- K080642 Comprehensive Reverse Shoulder2 generations on · 2008
Most influential descendants
Showing 5 of 248 · See all- K061439Aequalis Reversed ProsthesisTornier · 2006 · cites it directly199descendants
- K063569Equinoxe Reverse Shoulder SystemExactech, Inc. · 2007 · cites it directly190descendants
- K081059Aequalis Reversed Shoulder ProsthesisTornier · 2008 · cites it directly179descendants
- K071948Aequalis Reversed AdapterTornier · 2007 · cites it directly178descendants
- K073688Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and Locking ScrewExactech, Inc. · 2008 · 2 generations on177descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −6 | K911686 | Global Total Shoulder, Uncement Humeral Hemi-Shoul | Depuy, Inc. | 1991 | — |
| −5 | K984541 | Global FX Humeral Stem, Global Advantage Humeral Head | DePuy Orthopaedics, Inc. | 1999 | — |
| −4 | K992065 | Global Advantage Shoulder, Global Advantage Humeral Stem, Global Advantage… | DePuy Orthopaedics, Inc. | 1999 | — |
| −3 | K021478 | Delta Shoulder | Depuy, Inc. | 2003 | — |
| −2 | K030941 | Aequalis Reversed Shoulder Prosthesis | Tornier | 2004 | — |
| −1 | K041873 | Aequalis Reversed Shoulder Prosthesis | Tornier | 2004 | — |
| 0 (this device) | K050316 | Aequalis Reversed Shoulder Prosthesis | Tornier | 2005 | — |
| +1 | K061439 | Aequalis Reversed Prosthesis | Tornier | 2006 | — |
| +1 | K063569 | Equinoxe Reverse Shoulder System | Exactech, Inc. | 2007 | 13 |
| +1 | K081059 | Aequalis Reversed Shoulder Prosthesis | Tornier | 2008 | — |
| +1 | K071948 | Aequalis Reversed Adapter | Tornier | 2007 | — |
| +2 | K073688 | Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and Locking Screw | Exactech, Inc. | 2008 | 1 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1980 | 2 | 0 |
| 1992 | 1 | 0 |
| 1995 | 1 | 0 |
| 1998 | 1 | 0 |
| 1999 | 2 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 1 | 0 |
| 2007 | 2 | 0 |
| 2008 | 5 | 1 |
| 2010 | 6 | 0 |
| 2011 | 6 | 0 |
| 2012 | 8 | 0 |
| 2013 | 11 | 0 |
| 2014 | 10 | 0 |
| 2015 | 6 | 0 |
| 2016 | 7 | 0 |
| 2017 | 15 | 0 |
| 2018 | 18 | 0 |
| 2019 | 17 | 0 |
| 2020 | 19 | 0 |
| 2021 | 25 | 0 |
| 2022 | 19 | 0 |
| 2023 | 16 | 0 |
| 2024 | 17 | 0 |
| 2025 | 16 | 0 |
| 2026 | 24 | 0 |
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 K212737 INHANCE™ Reverse Shoulder Systemscore 28.4 · 15 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (5)
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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | K030941 | Aequalis Reversed Shoulder ProsthesisSummary page 1…KWS § 888.3660 Shoulderjoint metal/polymer semi-constrained cemented prosthesis. 5) Equivalent I Predicate device Aequalis Reversed Shoulder Prosthesis, TORNIER SA, K03 0941, K041873 Aequalis Shoulder System, TORNIER SA, K952928 Bipolar Shoulder Prosthesis, BIOMET Inc, K(991585 Delta Shoulder, DePuy In… | 2004 |
| * | K041873 | Aequalis Reversed Shoulder ProsthesisSummary page 1…888.3660 Shoulderjoint metal/polymer semi-constrained cemented prosthesis. 5) Equivalent I Predicate device Aequalis Reversed Shoulder Prosthesis, TORNIER SA, K03 0941, K041873 Aequalis Shoulder System, TORNIER SA, K952928 Bipolar Shoulder Prosthesis, BIOMET Inc, K(991585 Delta Shoulder, DePuy Inc, K02147… | 2004 |
| * | K952928 | Aequalis Shoulder System for Total & Hemishoulder ApplicationsSummary page 1…trained cemented prosthesis. 5) Equivalent I Predicate device Aequalis Reversed Shoulder Prosthesis, TORNIER SA, K03 0941, K041873 Aequalis Shoulder System, TORNIER SA, K952928 Bipolar Shoulder Prosthesis, BIOMET Inc, K(991585 Delta Shoulder, DePuy Inc, K021478 6) Device description The .equalis Reversed… | 1995 |
| * | K991585 | Bipolar Shoulder ProsthesisSummary page 1…cate device Aequalis Reversed Shoulder Prosthesis, TORNIER SA, K03 0941, K041873 Aequalis Shoulder System, TORNIER SA, K952928 Bipolar Shoulder Prosthesis, BIOMET Inc, K(991585 Delta Shoulder, DePuy Inc, K021478 6) Device description The .equalis Reversed Shoulder Prosthesis is intended to be used to rel… | 1999 |
| * | K021478 | Delta ShoulderSummary page 1…lder Prosthesis, TORNIER SA, K03 0941, K041873 Aequalis Shoulder System, TORNIER SA, K952928 Bipolar Shoulder Prosthesis, BIOMET Inc, K(991585 Delta Shoulder, DePuy Inc, K021478 6) Device description The .equalis Reversed Shoulder Prosthesis is intended to be used to relieve pain and significant disabilit… | 2003 |
What descends from it? (248)
See all 2489 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K061439 | Aequalis Reversed Prosthesis | 2006 | 199 |
| K063569 | Equinoxe Reverse Shoulder System | 2007 | 190 |
| K081059 | Aequalis Reversed Shoulder Prosthesis | 2008 | 179 |
| K071948 | Aequalis Reversed Adapter | 2007 | 178 |
| K082120 | Aequalis Reversed Fracture Shoulder Prothesis | 2008 | 164 |
| K100142 | Aequalis Reversed Shoulder Prosthesis | 2010 | 147 |
| K132285 | Aequalis Reversed Shoulder Prosthesis | 2013 | 26 |
| K112144 | Aequalis Shoulder Fracture System, Aequalis Reversed Shoulder Prosthesis, Aequalis… | 2012 | 23 |
| K151293 | Aequalis Ascend Flex Shoulder System, Aequalis Reversed Shoulder Prosthesis | 2015 | 20 |
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 on · ◆ in the 2008 descendants bar of FIG. 11 Class I recall
What does this lineage say?
- The line of descent spans 14 years and passes through 3 companies; a new generation was cleared every 7 months on median.
- 1 of the 13 ancestors has a recall of any class.
- Of its descendants, K061439 (Tornier, 2006) has gone furthest, with 199 descendants of its own.
- 16 other devices also cite its predicate K030941.
How does its category compare?
All PHX devicesPHX Shoulder Prosthesis, Reverse Configuration: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · PHX
9in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · PHX
72in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · PHX
3in 2025
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · PHX
2,848in 2025
MAUDE reports naming product code PHX, not matched to any one device; reports are not rates.
View these four charts as a table
| Year | Decisions | Median 510(k) review, days | Recalls (Class I) | MAUDE reports |
|---|---|---|---|---|
| 2007 | 5 | 97 | 0 | 0 |
| 2008 | 6 | 79 | 0 | 0 |
| 2009 | 1 | — | 0 | 0 |
| 2010 | 8 | 124 | 0 | 0 |
| 2011 | 12 | 94 | 0 | 0 |
| 2012 | 12 | 114 | 0 | 0 |
| 2013 | 8 | 143 | 0 | 0 |
| 2014 | 12 | 110 | 0 | 0 |
| 2015 | 4 | 206 | 2 | 14 |
| 2016 | 4 | 132 | 0 | 5 |
| 2017 | 11 | 141 | 0 | 25 |
| 2018 | 14 | 127 | 1 | 323 |
| 2019 | 9 | 144 | 3 | 504 |
| 2020 | 13 | 143 | 3 | 986 |
| 2021 | 21 | 143 | 8 | 1,404 |
| 2022 | 9 | 198 | 0 | 1,342 |
| 2023 | 9 | 154 | 7 | 1,401 |
| 2024 | 9 | 139 | 1 | 2,142 |
| 2025 | 9 | 72 | 3 | 2,848 |
| 2026 | 18 | 130 | 7 | — |
What is it indicated for?
The Aequalis Reversed Shoulder Prosthesis is indicated for patients with a functional deltoid muscle as a total shoulder replacement for the relief of pain and significant disability following arthropathy associated to massive and non repairable rotator cuff-tear. This device is also indicated for the prosthetic revisions with massive and non repairable rotator cuff-tear. Only the humeral components are for cemented use. The glenoid implant is anchored…
Read the full statement (200 words)
The Aequalis Reversed Shoulder Prosthesis is indicated for patients with a functional deltoid muscle as a total shoulder replacement for the relief of pain and significant disability following arthropathy associated to massive and non repairable rotator cuff-tear. This device is also indicated for the prosthetic revisions with massive and non repairable rotator cuff-tear. Only the humeral components are for cemented use. The glenoid implant is anchored to the bone with 4 screws and is for non-cemented fixation-
When during the primary surgery the glenoid bone stock appears to be insufficient to bear the reversed glenoid components or when glenoid bone fracture occurs during the surgical procedures, the hemi-prosthesis adaptor and the union screw can be adapted to the humeral components in order to transform the Aequalis Reversed prosthesis in to a non reversed hemi-prosthesis.
When, in case of revision of a Aequalis Reversed prosthesis, the glenoid bone stock appears to be insufficient to again implant a base plate and a sphere of Aequalis Reversed range, the use of the hemi-prosthesis adaptor and the union screw allows for the transformation of the Aequalis Reversed prosthesis in to a non reversed hemi-prosthesis in order to avoid the revision of the humeral components-
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K050316 · printed Nov 6, 2026
Cite this page
510(k) Report. “K050316: Aequalis Reversed Shoulder Prosthesis.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K050316
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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