510(k) · Cleared
ClearedAequalis Shoulder Fracture System & Aequalis Shoulder System
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Tornier · KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Cleared on Mar 2, 2006 as substantially equivalent to K952928 (Tornier, 1995) and 5 other predicates after a 34-day review. Its family tree reaches back 4 generations to 1993. 257 later devices descend from it.
- Decided
- Mar 2, 2006
- Review
- 34 days
- Class
- Class II
- Product code
- KWS
- Recalls
- None
- Predicates
- 6
Its longest line of descent runs back 4 generations to K920362 (1993). 10 ancestors in all, the oldest K873679 (1987). 257 later devices descend from it, 12 citing it directly.
- Root · 4 generations backK920362 3M Modular Shoulder System3M Health Care, Ltd. · 1993
- 3 generations backK002683 WMT Ultra-Fit Modular Shoulder SystemWrightmedicaltechnologyinc · 2000
- 2 generations backK032679 Aequalis Shoulder Fracture SystemTornier · 2003
- 1 generation backK043077 Modification to Aequalis Shoulder Fracture System; Aequalis Shoulder…Tornier · 2004
- This deviceK060209 Aequalis Shoulder Fracture System & Aequalis Shoulder SystemTornier · 2006
- Descendant · cites it directly · 199 of its ownK061439 Aequalis Reversed ProsthesisTornier · 2006
- Descendant · cites it directly · 179 of its ownK081059 Aequalis Reversed Shoulder ProsthesisTornier · 2008
- Descendant · 2 generations on · 178 of its ownK071948 Aequalis Reversed AdapterTornier · 2007
- Descendant · cites it directly · 164 of its ownK082120 Aequalis Reversed Fracture Shoulder ProthesisTornier · 2008
- Descendant · cites it directly · 162 of its ownK063081 Aequalis Shoulder SystemTornier · 2006
Showing 5 of 257 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 257 · See all- K061439Aequalis Reversed ProsthesisTornier · 2006 · cites it directly199descendants
- K081059Aequalis Reversed Shoulder ProsthesisTornier · 2008 · cites it directly179descendants
- K071948Aequalis Reversed AdapterTornier · 2007 · 2 generations on178descendants
- K082120Aequalis Reversed Fracture Shoulder ProthesisTornier · 2008 · cites it directly164descendants
- K063081Aequalis Shoulder SystemTornier · 2006 · cites it directly162descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −4 | K920362 | 3M Modular Shoulder System | 3M Health Care, Ltd. | 1993 | — |
| −3 | K002683 | WMT Ultra-Fit Modular Shoulder System | Wrightmedicaltechnologyinc | 2000 | — |
| −2 | K032679 | Aequalis Shoulder Fracture System | Tornier | 2003 | — |
| −1 | K043077 | Modification to Aequalis Shoulder Fracture System; Aequalis Shoulder System | Tornier | 2004 | — |
| 0 (this device) | K060209 | Aequalis Shoulder Fracture System & Aequalis Shoulder System | Tornier | 2006 | — |
| +1 | K061439 | Aequalis Reversed Prosthesis | Tornier | 2006 | — |
| +1 | K081059 | Aequalis Reversed Shoulder Prosthesis | Tornier | 2008 | — |
| +2 | K071948 | Aequalis Reversed Adapter | Tornier | 2007 | — |
| +1 | K082120 | Aequalis Reversed Fracture Shoulder Prothesis | Tornier | 2008 | — |
| +1 | K063081 | Aequalis Shoulder System | Tornier | 2006 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1987 | 1 | 0 |
| 1995 | 1 | 0 |
| 1996 | 1 | 0 |
| 2000 | 2 | 0 |
| 2004 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2006 | 4 | 0 |
| 2007 | 2 | 0 |
| 2008 | 3 | 0 |
| 2010 | 5 | 0 |
| 2011 | 10 | 0 |
| 2012 | 7 | 0 |
| 2013 | 8 | 0 |
| 2014 | 11 | 0 |
| 2015 | 6 | 0 |
| 2016 | 12 | 0 |
| 2017 | 14 | 0 |
| 2018 | 17 | 0 |
| 2019 | 20 | 0 |
| 2020 | 18 | 0 |
| 2021 | 22 | 0 |
| 2022 | 22 | 0 |
| 2023 | 17 | 0 |
| 2024 | 16 | 0 |
| 2025 | 21 | 0 |
| 2026 | 22 | 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.
Planning a device in KWS? 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 K220847 AETOS Shoulder Systemscore 21.1 · 16 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (6)
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 |
|---|---|---|---|
| * | K952928 | Aequalis Shoulder System for Total & Hemishoulder ApplicationsSummary page 1…panel: Orthopedic Product code: KWS 5) Equivalent / Predicate device For the AEQUALIS Shoulder Fracture System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077 AEQUALIS Shoulder Fracture system, TORNIER SA, K994392, K003728, K032679, K043077 For the AEQUALIS Shoulder Sy… | 1995 |
| * | K041339 | Aequalis Shoulder SystemSummary page 1…Orthopedic Product code: KWS 5) Equivalent / Predicate device For the AEQUALIS Shoulder Fracture System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077 AEQUALIS Shoulder Fracture system, TORNIER SA, K994392, K003728, K032679, K043077 For the AEQUALIS Shoulder System: AEQ… | 2004 |
| * | K043077 | Modification to Aequalis Shoulder Fracture System; Aequalis Shoulder SystemSummary page 1…pedic Product code: KWS 5) Equivalent / Predicate device For the AEQUALIS Shoulder Fracture System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077 AEQUALIS Shoulder Fracture system, TORNIER SA, K994392, K003728, K032679, K043077 For the AEQUALIS Shoulder System: AEQUALIS Sho… | 2004 |
| * | K994392 | Aequalis Shoulder Fracture SystemSummary page 1…redicate device For the AEQUALIS Shoulder Fracture System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077 AEQUALIS Shoulder Fracture system, TORNIER SA, K994392, K003728, K032679, K043077 For the AEQUALIS Shoulder System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077… | 2000 |
| * | K003728 | Modification to Aequalis Shoulder Fracture SystemSummary page 1…device For the AEQUALIS Shoulder Fracture System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077 AEQUALIS Shoulder Fracture system, TORNIER SA, K994392, K003728, K032679, K043077 For the AEQUALIS Shoulder System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077… | 2000 |
| * | K032679 | Aequalis Shoulder Fracture SystemSummary page 1…r the AEQUALIS Shoulder Fracture System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077 AEQUALIS Shoulder Fracture system, TORNIER SA, K994392, K003728, K032679, K043077 For the AEQUALIS Shoulder System: AEQUALIS Shoulder system, TORNIER SA, K952928, K041339, K043077… | 2003 |
What descends from it? (257)
See all 25712 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 |
| K081059 | Aequalis Reversed Shoulder Prosthesis | 2008 | 179 |
| K082120 | Aequalis Reversed Fracture Shoulder Prothesis | 2008 | 164 |
| K063081 | Aequalis Shoulder System | 2006 | 162 |
| K111902 | Aequalis Shoulder System | 2011 | 49 |
| K081707 | Aequalis Shoulder Fracture and Shoulder Systems | 2008 | 25 |
| K112144 | Aequalis Shoulder Fracture System, Aequalis Reversed Shoulder Prosthesis, Aequalis… | 2012 | 23 |
| K062661 | Aequalis Resurfacing Head | 2006 | 16 |
| K062029 | Anatomical Shoulder Fracture System | 2006 | 10 |
| K131231 | Aequalis Shoulder Fracture System, Aequalis Reversed Shoulder Prosthesis, Aequalis… | 2013 | 5 |
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 13 years and passes through 3 companies; a new generation was cleared every 3.1 years on median.
- None of the 10 ancestors has a recall.
- Of its descendants, K061439 (Tornier, 2006) has gone furthest, with 199 descendants of its own.
- 18 other devices also cite its predicate K952928.
How does its category compare?
All KWS devicesKWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KWS
3in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KWS
97in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KWS
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KWS
2,281in 2025
MAUDE reports naming product code KWS, 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 | 2 | — | 21 | 158 |
| 2008 | 4 | 37 | 29 | 238 |
| 2009 | 4 | 108 | 0 | 294 |
| 2010 | 7 | 33 | 10 | 393 |
| 2011 | 11 | 90 | 11 | 486 |
| 2012 | 7 | 86 | 10 | 542 |
| 2013 | 12 | 120 | 0 | 818 |
| 2014 | 7 | 89 | 1 | 1,066 |
| 2015 | 8 | 129 | 0 | 1,170 |
| 2016 | 10 | 114 | 1 | 970 |
| 2017 | 7 | 120 | 4 | 1,681 |
| 2018 | 4 | 152 | 1 | 1,545 |
| 2019 | 9 | 106 | 2 | 1,728 |
| 2020 | 3 | 98 | 5 | 1,567 |
| 2021 | 5 | 151 | 0 | 1,358 |
| 2022 | 5 | 158 | 0 | 1,268 |
| 2023 | 4 | 250 | 2 | 1,750 |
| 2024 | 2 | — | 0 | 2,122 |
| 2025 | 3 | 97 | 0 | 2,281 |
| 2026 | 2 | — | 1 | — |
What is it indicated for?
AEQUALIS Shoulder Range (except AEQUALIS for Fracture): Prosthetic replacement with this device may be indicated to relieve severe pain or significant disability caused by: - Degenerative pathologies : arthrosis, rheumatoid arthritis, post-traumatic arthrosis. Primary and secondary necrosis of the humeral head - Displaced 4-part upper humeral fracture - lumeral head fracture - Other pathologies where arthrodesis or resectional arthroplasty of the humeral…
Read the full statement (113 words)
AEQUALIS Shoulder Range (except AEQUALIS for Fracture):
Prosthetic replacement with this device may be indicated to relieve severe pain or significant disability caused by:
- Degenerative pathologies : arthrosis, rheumatoid arthritis, post-traumatic arthrosis. Primary and secondary necrosis of the humeral head
- Displaced 4-part upper humeral fracture
- lumeral head fracture
- Other pathologies where arthrodesis or resectional arthroplasty of the humeral head are not acceptable
- Revision surgery when other treatments or devices have failed.
AEQUALIS for Fracture:
Traumatic or pathologic conditions of the shoulder resulting in fracture of the glenohumeral joint, including humeral head fracture and displaced 3-or 4-part proximal humeral fractures.
Revision surgery when other treatments or devices have failed.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K060209 · printed Nov 6, 2026
Cite this page
510(k) Report. “K060209: Aequalis Shoulder Fracture System & Aequalis 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/K060209
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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