510(k) Report

510(k) · Cleared

Cleared

AETOS Shoulder System

K230572510(k) TraditionalCleared Jun 7, 202398-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

Smith & Nephew, Inc. · KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Cleared on Jun 7, 2023 as substantially equivalent to K220847 (Smith & Nephew, Inc., 2023) and 2 other predicates after a 98-day review. Its family tree reaches back 18 generations to 1991. 1 of the 193 devices in its family, counting itself, has a Class I recall. 1 later device descends from it.

Decided
Jun 7, 2023
Review
98 days
Class
Class II
Product code
KWS
Recalls
None
Predicates
3

Its longest line of descent runs back 18 generations to K911686 (1991). 191 ancestors in all, the oldest K790987 (1979). 1 later device descends from it, 1 citing it directly. 1 of the 193 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2023: 1 other ancestor2020: 1 other ancestor2019: 2 other ancestors2018: 1 other ancestor2016: 2 other ancestors2008: 10 other ancestors2015: 1 other ancestor2014: 4 other ancestors2013: 2 other ancestors2012: 8 other ancestors2011: 11 other ancestors2010: 8 other ancestors2009: 3 other ancestors2007: 7 other ancestors2006: 12 other ancestors2005: 8 other ancestors2004: 8 other ancestors2003: 7 other ancestors2002: 4 other ancestors2001: 10 other ancestors2000: 12 other ancestors1999: 6 other ancestors1997: 3 other ancestors1995: 3 other ancestors1998: 6 other ancestors1996: 10 other ancestors1994: 6 other ancestors1992: 2 other ancestors1988: 1 other ancestor1987: 5 other ancestors1980: 2 other ancestors1991: 3 other ancestors1993: 1 other ancestor1989: 1 other ancestor1986: 1 other ancestor1979: 1 other ancestor2025: 1 descendant clearedReference device: K172351 · AltiVate Reverse Humeral Stem, AltiVate Reverse Small Spacer, Altivate Reverse, Small Hemi-Adapter, AltiVate Reverse, Small Socket Insert · Encore Medical L.P. · 2017 · recalledReference device: K052906 · Zimmer Trabecular Metal Reverse Shoulder System · Zimmer, Inc. · 2005 · recalledReference device: K130129 · Univers Revers Shoulder Prosthesis System · Arthrex, Inc. · 2013Reference device: K210717 · Bone Screws dia. 5,0 mm · Lima Corporate S.P.A. · 2021Reference device: K142139 · SMR 40MM Glenosphere · Lima Corporate S.P.A. · 2014Reference device: K130050 · Titan Reverse Shoulder System · Ascension Orthopedic · 2013Reference device: K181999 · Integra TITAN Reverse Shoulder System · Integra LifeSciences Corporation · 2018Reference device: K152047 · INTEGRA TITAN Modular Total Shoulder System Fin-Lock Glenoid · Ascension Orthopedics · 2015K911686 · 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 · recalled×2: 2 generations cleared close together, K073688 (2008), K080642 (2008) ×2: 2 generations cleared close together, K110599 (2011), K112615 (2011) K122698 · Aequalis Ascend Flex Shoulder System · Tornier S.A.S. · 2013 · recalledK132285 · Aequalis Reversed Shoulder Prosthesis · Tornier S.A.S. · 2013K151293 · Aequalis Ascend Flex Shoulder System, Aequalis Reversed Shoulder Prosthesis · Tornier S.A.S. · 2015K190521 · Aequalis Ascend Flex Shoulder System · Tornier S.A.S. · 2019K201315 · PERFORM Humeral System – Stem · Tornier, Inc. · 2020 · recalled19801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 2 other ancestors2 generations back: 6 other ancestors3 generations back: 21 other ancestors4 generations back: 30 other ancestors5 generations back: 56 other ancestors6 generations back: 18 other ancestors7 generations back: 23 other ancestors8 generations back: 10 other ancestors9 generations back: 6 other ancestors10 generations back: 1 other ancestor 1 generation forward: 1 descendant K201315 · PERFORM Humeral System – Stem · Tornier, Inc. · 2020 · recalledK190521 · Aequalis Ascend Flex Shoulder System · Tornier S.A.S. · 2019K151293 · Aequalis Ascend Flex Shoulder System, Aequalis Reversed Shoulder Prosthesis · Tornier S.A.S. · 2015K132285 · Aequalis Reversed Shoulder Prosthesis · Tornier S.A.S. · 2013K122698 · Aequalis Ascend Flex Shoulder System · Tornier S.A.S. · 2013 · recalledK112615 · Aequalis Ascend Modular Reverse Shoulder System · Tornier, Inc. · 2011K110599 · Aequalis Ascend Modular Reverse Shoulder System · Tornier, Inc. · 2011K080642 · 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. · 1991−15−10−50
  1. Root · 18 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
  2. 14 generations between
  3. 3 generations backK151293 Aequalis Ascend Flex Shoulder System, Aequalis Reversed Shoulder…Tornier S.A.S. · 2015
  4. 2 generations backK190521 Aequalis Ascend Flex Shoulder SystemTornier S.A.S. · 2019
  5. 1 generation backK201315 PERFORM Humeral System – StemTornier, Inc. · 2020 · Recalled
  6. This deviceK230572 AETOS Shoulder SystemSmith & Nephew, Inc. · 2023
  7. Descendant · cites it directly · 0 of its ownK252416 AETOS Shoulder System Meta Humeral Prosthesis Size 0Smith & Nephew, Inc. · 2025
Show all 18 generations
  1. Root · 18 generations backK911686 Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc. · 1991
  2. 17 generations backK984541 Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc. · 1999
  3. 16 generations backK992065 Global Advantage Shoulder, Global Advantage Humeral Stem, Global…DePuy Orthopaedics, Inc. · 1999
  4. 15 generations backK021478 Delta ShoulderDepuy, Inc. · 2003
  5. 14 generations backK030941 Aequalis Reversed Shoulder ProsthesisTornier · 2004
  6. 13 generations backK041873 Aequalis Reversed Shoulder ProsthesisTornier · 2004
  7. 12 generations backK052906 Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc. · 2005 · Recalled
  8. 11 generations backK060704 Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc. · 2006 · Recalled
  9. 10 generations backK063569 Equinoxe Reverse Shoulder SystemExactech, Inc. · 2007 · Recalled
  10. 9 generations backK073688 Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and…Exactech, Inc. · 2008 · Recalled
  11. 8 generations backK080642 Comprehensive Reverse ShoulderBiomet, Inc. · 2008 · Recalled (Class I)
  12. 7 generations backK110599 Aequalis Ascend Modular Reverse Shoulder SystemTornier, Inc. · 2011
  13. 6 generations backK112615 Aequalis Ascend Modular Reverse Shoulder SystemTornier, Inc. · 2011
  14. 5 generations backK122698 Aequalis Ascend Flex Shoulder SystemTornier S.A.S. · 2013 · Recalled
  15. 4 generations backK132285 Aequalis Reversed Shoulder ProsthesisTornier S.A.S. · 2013
  16. 3 generations backK151293 Aequalis Ascend Flex Shoulder System, Aequalis Reversed Shoulder…Tornier S.A.S. · 2015
  17. 2 generations backK190521 Aequalis Ascend Flex Shoulder SystemTornier S.A.S. · 2019
  18. 1 generation backK201315 PERFORM Humeral System – StemTornier, Inc. · 2020 · Recalled
  19. This deviceK230572 AETOS Shoulder SystemSmith & Nephew, Inc. · 2023

Class I recalls in this family

Most influential descendants

Showing 1 of 1 · See all
  • K252416AETOS Shoulder System Meta Humeral Prosthesis Size 0Smith & Nephew, Inc. · 2025 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−18K911686Global Total Shoulder, Uncement Humeral Hemi-ShoulDepuy, Inc.1991—
−17K984541Global FX Humeral Stem, Global Advantage Humeral HeadDePuy Orthopaedics, Inc.1999—
−16K992065Global Advantage Shoulder, Global Advantage Humeral Stem, Global Advantage…DePuy Orthopaedics, Inc.1999—
−15K021478Delta ShoulderDepuy, Inc.2003—
−14K030941Aequalis Reversed Shoulder ProsthesisTornier2004—
−13K041873Aequalis Reversed Shoulder ProsthesisTornier2004—
−12K052906Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc.200512
−11K060704Zimmer Trabecular Metal Reverse Shoulder System, Sizes 8MM and 10MMZimmer, Inc.200610
−10K063569Equinoxe Reverse Shoulder SystemExactech, Inc.200713
−9K073688Equinoxe Reverse Shoulder System Fracture Humeral Adapter Tray and Locking ScrewExactech, Inc.20081
−8K080642Comprehensive Reverse ShoulderBiomet, Inc.2008Class I
−7K110599Aequalis Ascend Modular Reverse Shoulder SystemTornier, Inc.2011—
−6K112615Aequalis Ascend Modular Reverse Shoulder SystemTornier, Inc.2011—
−5K122698Aequalis Ascend Flex Shoulder SystemTornier S.A.S.20132
−4K132285Aequalis Reversed Shoulder ProsthesisTornier S.A.S.2013—
−3K151293Aequalis Ascend Flex Shoulder System, Aequalis Reversed Shoulder ProsthesisTornier S.A.S.2015—
−2K190521Aequalis Ascend Flex Shoulder SystemTornier S.A.S.2019—
−1K201315PERFORM Humeral System – StemTornier, Inc.20201
0 (this device)K230572AETOS Shoulder SystemSmith & Nephew, Inc.2023—
+1K252416AETOS Shoulder System Meta Humeral Prosthesis Size 0Smith & Nephew, Inc.2025—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
197910
198020
198610
198750
198810
198910
199130
199220
199310
199460
199530
1996100
199730
199860
199960
2000120
2001100
200240
200370
200480
200580
2006120
200770
2008100
200930
201080
2011110
201280
201320
201440
201510
201620
201810
201920
202010
202310

Descendants by year cleared

Year clearedDevicesWith a Class I recall
202510
FIG. 1 — Lineage of K230572, 1991–2025Source: 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.

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 KWS device

  1. #1 K220847 AETOS Shoulder Systemscore 21.1 · 16 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? (3)

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
*K220847AETOS Shoulder System
Summary page 5
…ymer semi-constrained cemented prosthesis (21 CFR 888.3660) Classification Class II Predicate Devices Smith & Nephew AETOS Shoulder System: K220847 (Primary) Tornier, Inc. PERFORM Humeral System - Stem: K201315 LimaCorporate SMR TT Augme…
Smith & Nephew, Inc.2023—
*K201315PERFORM Humeral System – Stem
Summary page 5
…Classification Class II Predicate Devices Smith & Nephew AETOS Shoulder System: K220847 (Primary) Tornier, Inc. PERFORM Humeral System - Stem: K201315 LimaCorporate SMR TT Augmented Glenoid System: K200171 Reference Devices Encore AltiVate Reverse Humeral St…
Tornier, Inc.20201
*K200171SMR TT Augmented Glenoid System
Summary page 5
…der System: K220847 (Primary) Tornier, Inc. PERFORM Humeral System - Stem: K201315 LimaCorporate SMR TT Augmented Glenoid System: K200171 Reference Devices Encore AltiVate Reverse Humeral Stem, AltiVate Reverse Small Spacer, Altivate Reverse, Sm…
Lima Corporate S.P.A.2020—
†K172351AltiVate Reverse Humeral Stem, AltiVate Reverse Small Spacer, Altivate Reverse, Small…Encore Medical L.P.20173
†K052906Zimmer Trabecular Metal Reverse Shoulder SystemZimmer, Inc.200512
†K130129Univers Revers Shoulder Prosthesis SystemArthrex, Inc.2013—
†K210717Bone Screws dia. 5,0 mmLima Corporate S.P.A.2021—
†K142139SMR 40MM GlenosphereLima Corporate S.P.A.2014—
†K130050Titan Reverse Shoulder SystemAscension Orthopedic2013—
†K181999Integra TITAN Reverse Shoulder SystemIntegra LifeSciences Corporation2018—
†K152047INTEGRA TITAN Modular Total Shoulder System Fin-Lock GlenoidAscension Orthopedics2015—

Also cleared against K220847: 3 other devices →

What descends from it? (1)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K252416AETOS Shoulder System Meta Humeral Prosthesis Size 0Smith & Nephew, Inc.20250

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 · 3 generations back · ◆ on the line of descent in FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 32 years and passes through 9 companies; a new generation was cleared every 1.2 years on median.
  • 55 of the 191 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K252416 (Smith & Nephew, Inc., 2025) has gone furthest, with 0 descendants of its own.
  • 3 other devices also cite its predicate K220847.

How does its category compare?

All KWS devices

KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented: FDA decisions, review times, recalls and adverse event reports over 20 years. 2023, this device’s year, is highlighted.

FDA decisions per year · KWS

3in 2025

2007: 22008: 42009: 42010: 72011: 112012: 72013: 122014: 72015: 82016: 102017: 72018: 42019: 92020: 32021: 52022: 52023: 42024: 22025: 32026 (partial year): 2
2007high 12 (2013) · low 2 (2007)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · KWS

97in 2025

2008: 37 days median2009: 108 days median2010: 33 days median2011: 90 days median2012: 86 days median2013: 120 days median2014: 89 days median2015: 129 days median2016: 114 days median2017: 120 days median2018: 152 days median2019: 106 days median2020: 98 days median2021: 151 days median2022: 158 days median2023: 250 days median2025: 97 days median
2007high 250 (2023) · low 33 (2010)2026

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

Recalls per year · KWS

2in 2023

2007: 212008: 292010: 102011: 112012: 102014: 12016: 12017: 42018: 12019: 22020: 52023: 22026 (partial year): 1
2007high 29 (2008) · low 0 (2009)2026

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

Adverse event reports per year · KWS

2,281in 2025

2007: 1582008: 2382009: 2942010: 3932011: 4862012: 5422013: 8182014: 1,0662015: 1,1702016: 9702017: 1,6812018: 1,5452019: 1,7282020: 1,5672021: 1,3582022: 1,2682023: 1,7502024: 2,1222025: 2,281
2007high 2,281 (2025) · low 158 (2007)2025

MAUDE reports naming product code KWS, 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
20072—21158
200843729238
200941080294
201073310393
2011119011486
201278610542
2013121200818
201478911,066
2015812901,170
2016101141970
2017712041,681
2018415211,545
2019910621,728
202039851,567
2021515101,358
2022515801,268
2023425021,750
20242—02,122
202539702,281
20262—1—

What is it indicated for?

In Anatomic: The stem and head may be used by themselves, as a hemiarthroplasty, if the natural glenoid provides a sufficient bearing surface, or in conjunction with the glenoid, as a total replacement. The AETOS Shoulder System is to be used only in patients with an intact or reconstructable rotator cuff, where it is intended to provide increased mobility and stability and to relieve pain. The AETOS Shoulder System is indicated for use as a replacement…

Read the full statement (324 words)

In Anatomic:

The stem and head may be used by themselves, as a hemiarthroplasty, if the natural glenoid provides a sufficient bearing

surface, or in conjunction with the glenoid, as a total replacement.

The AETOS Shoulder System is to be used only in patients with an intact or reconstructable rotator cuff, where it is

intended to provide increased mobility and stability and to relieve pain. The AETOS Shoulder System is indicated for use

as a replacement of shoulder joints disabled by:

• Rheumatoid arthritis

• Non-inflammatory degenerative joint disease

• Correction of functional deformity

• Fractures of the humeral head

• Traumatic arthritis

• Revision of other devices if sufficient bone stock remains

The coated humeral component is intended for uncemented use. The glenoid component is intended for cemented use

only.

In Reverse:

The AETOS Shoulder System is indicated for use as a replacement of shoulder joints for patients with a functional deltoid

muscle and with massive and non-repairable rotator cuff-tear with pain disabled by:

• Rheumatoid arthritis

• Non-inflammatory degenerative joint disease

• Correction of functional deformity

• Fractures of the humeral head

• Traumatic arthritis

• Revision of devices if sufficient bone stock remains

The humeral liner component is indicated for use in the AETOS Shoulder System as a primary reverse total shoulder

replacement and for use when converting an anatomic AETOS Shoulder System into a reverse shoulder construct. This

facilitates the conversion without the removal of the humeral stem during revision surgery for patients with a functional

deltoid muscle. The component is permitted to be used in the conversion from anatomic to reverse if the humeral stem is

well fixed, the patient has a functional deltoid muscle; the arthroplasty is associated with a massive and non-repairable

rotator cuff tear.

The coated humeral stem is indicated for uncemented use. The coated glenoid baseplate is intended for cementless

application with the addition of screws for fixation.

Note: All implant components are single use.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K230572: AETOS 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/K230572

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