510(k) · Cleared
Recalled · 2005The Trabecular Metal Glenoid-Bigliani/Flatow the Complete Shoulder Solution, Model 4306
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Implex Corp. · KWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented
Cleared on Dec 10, 2002 after a 141-day review. The FDA summary names its predicate without a number. 65 later devices descend from it. It has been recalled 8 times.
- Decided
- Dec 10, 2002
- Review
- 141 days
- Class
- Class II
- Product code
- KWT
- Recalls
- 8
- Predicates
- 0
65 later devices descend from it, 5 citing it directly.
- This deviceK022377 The Trabecular Metal Glenoid-Bigliani/Flatow the Complete Shoulder…Implex Corp. · 2002
- Descendant · cites it directly · 60 of its ownK031449 Modification to the Trabecular Metal Glenoid - Bigliani/Flatow the…Implex Corp. · 2003 · Recalled
- Descendant · cites it directly · 58 of its ownK043061 The Trabecular Metal Glenoid - Bigliani/Flatow the Complete Shoulder…Zimmer Trabecular · 2004
- Descendant · cites it directly · 57 of its ownK060694 Modular Hybrid GlenoidBiomet Manufacturing Corp · 2006 · Recalled
- Descendant · 2 generations on · 24 of its ownK093430 Exactech Equinoxe XL Keeled Glenoid, Pegged Glenoid, Exactech…Exactech, Inc. · 2010 · Recalled
- Descendant · 2 generations on · 23 of its ownK091196 GRS Glenoid Resurfacing SystemArthrosurface, Inc. · 2009
Showing 5 of 65 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 65 · See all- K031449Modification to the Trabecular Metal Glenoid - Bigliani/Flatow the Complete Shoulder…Implex Corp. · 2003 · cites it directly60descendants
- K043061The Trabecular Metal Glenoid - Bigliani/Flatow the Complete Shoulder Solution, Model…Zimmer Trabecular · 2004 · cites it directly58descendants
- K060694Modular Hybrid GlenoidBiomet Manufacturing Corp · 2006 · cites it directly57descendants
- K093430Exactech Equinoxe XL Keeled Glenoid, Pegged Glenoid, Exactech Equinoxe Cage, Glenoid…Exactech, Inc. · 2010 · 2 generations on24descendants
- K091196GRS Glenoid Resurfacing SystemArthrosurface, Inc. · 2009 · 2 generations on23descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K022377 | The Trabecular Metal Glenoid-Bigliani/Flatow the Complete Shoulder Solution… | Implex Corp. | 2002 | — |
| +1 | K031449 | Modification to the Trabecular Metal Glenoid - Bigliani/Flatow the Complete… | Implex Corp. | 2003 | 8 |
| +1 | K043061 | The Trabecular Metal Glenoid - Bigliani/Flatow the Complete Shoulder Solution… | Zimmer Trabecular | 2004 | — |
| +1 | K060694 | Modular Hybrid Glenoid | Biomet Manufacturing Corp | 2006 | 4 |
| +2 | K093430 | Exactech Equinoxe XL Keeled Glenoid, Pegged Glenoid, Exactech Equinoxe Cage… | Exactech, Inc. | 2010 | 1 |
| +2 | K091196 | GRS Glenoid Resurfacing System | Arthrosurface, Inc. | 2009 | — |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2003 | 1 | 0 |
| 2004 | 1 | 0 |
| 2006 | 1 | 0 |
| 2007 | 1 | 0 |
| 2009 | 1 | 0 |
| 2010 | 2 | 0 |
| 2011 | 3 | 0 |
| 2012 | 1 | 0 |
| 2015 | 1 | 0 |
| 2016 | 2 | 0 |
| 2017 | 2 | 0 |
| 2018 | 4 | 0 |
| 2019 | 5 | 0 |
| 2020 | 2 | 0 |
| 2021 | 2 | 0 |
| 2022 | 9 | 0 |
| 2023 | 6 | 0 |
| 2024 | 5 | 0 |
| 2025 | 6 | 0 |
| 2026 | 10 | 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 KWT? 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 KWT device
- #1 K231657 AGILON® XO Shoulder Replacement Systemscore 17.7 · 17 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the 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.
| Type | Number | Device | Decided |
|---|---|---|---|
| * | — | B/F all-poly glenoid components Named without a submission number | |
| † | K982981 | New Zimmer Shoulder System | 1998 |
What descends from it? (65)
See all 655 later devices cite it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K031449 | Modification to the Trabecular Metal Glenoid - Bigliani/Flatow the Complete Shoulder… | 2003 | 60 |
| K043061 | The Trabecular Metal Glenoid - Bigliani/Flatow the Complete Shoulder Solution, Model… | 2004 | 58 |
| K060694 | Modular Hybrid Glenoid | 2006 | 57 |
| K071090 | Trabecular Metal Glenoid- B/F Complete Shoulder Solution | 2007 | 13 |
| K103404 | ANA0TOMICAL Shoulder TM Combined System | 2011 | 3 |
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Aug 23, 2005 | Not classified | Z-0023-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0024-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0026-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0030-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0027-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0029-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0025-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
| Aug 23, 2005 | Not classified | Z-0028-06 | Other | The implant may fracture at the junction of the base and the trabecular metal keel if adequate support for the base has not been achieved by the host bone and/or bone cement. |
The 5 latest of 8 recalls; the web page lists all.
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K031449 (Implex Corp., 2003) has gone furthest, with 60 descendants of its own.
How does its category compare?
All KWT devicesKWT Prosthesis, Shoulder, Non-Constrained, Metal/Polymer Cemented: FDA decisions, review times, recalls and adverse event reports over 20 years.
FDA decisions per year · KWT
4in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · KWT
242in 2025
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · KWT
1in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · KWT
749in 2025
MAUDE reports naming product code KWT, 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 | 1 | — | 0 | 32 |
| 2008 | 0 | — | 1 | 48 |
| 2009 | 0 | — | 0 | 58 |
| 2010 | 1 | — | 7 | 71 |
| 2011 | 5 | 165 | 0 | 112 |
| 2012 | 1 | — | 2 | 83 |
| 2013 | 1 | — | 1 | 113 |
| 2014 | 1 | — | 0 | 168 |
| 2015 | 2 | — | 0 | 176 |
| 2016 | 2 | — | 1 | 445 |
| 2017 | 1 | — | 1 | 560 |
| 2018 | 2 | — | 1 | 480 |
| 2019 | 4 | 91 | 3 | 419 |
| 2020 | 1 | — | 0 | 215 |
| 2021 | 1 | — | 0 | 228 |
| 2022 | 1 | — | 0 | 273 |
| 2023 | 1 | — | 1 | 361 |
| 2024 | 1 | — | 0 | 601 |
| 2025 | 4 | 242 | 0 | 749 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
Prosthetic replacement with this device may be indicated for the treatment of severe pain or significant disability in degenerative, rheumatoid, or traumatic disease of the glenohumeral joint; un-united humeral head fractures of long duration; irreducible 3- and 4-part proximal humeral fractures; avascular necrosis of the humeral head; or other difficult clinical management problems where arthrodesis or resectional arthroplasty is not acceptable. The…
Read the full statement (122 words)
Prosthetic replacement with this device may be indicated for the treatment of severe pain or significant disability in degenerative, rheumatoid, or traumatic disease of the glenohumeral joint; un-united humeral head fractures of long duration; irreducible 3- and 4-part proximal humeral fractures; avascular necrosis of the humeral head; or other difficult clinical management problems where arthrodesis or resectional arthroplasty is not acceptable. The assembled humeral component may be used alone for hemiarthroplasty or combined with the glenoid component for total shoulder arthroplasty. Humeral heads with heights greater than 27 mm may be used for difficult clinical management problems involving rotator cuff deficiency where arthrodesis or conventional non-constrained arthroplasty is not acceptable. The Trabecular Metal Glenoid must be cemented in place in the USA.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K022377 · printed Nov 6, 2026
Cite this page
510(k) Report. “K022377: The Trabecular Metal Glenoid-Bigliani/Flatow the Complete Shoulder Solution, Model 4306.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K022377
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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