510(k) · Cleared
Recalled · Class II · 2012Anatomica Glenoid Component
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Sulzer Orthopedics, Inc. · KWS Prosthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented
Cleared on Mar 1, 1999 after a 46-day review. The FDA summary names its predicate without a number. 135 later devices descend from it. It has been recalled 2 times.
- Decided
- Mar 1, 1999
- Review
- 46 days
- Class
- Class II
- Product code
- KWS
- Recalls
- 2
- Predicates
- 0
135 later devices descend from it, 4 citing it directly.
- This deviceK990136 Anatomica Glenoid ComponentSulzer Orthopedics, Inc. · 1999
- Descendant · cites it directly · 130 of its ownK032126 Promos ShoulderPlus Orthopedics · 2004
- Descendant · cites it directly · 71 of its ownK042021 Exactech Equinoxe Shoulder SystemExactech, Inc. · 2004 · Recalled
- Descendant · 2 generations on · 67 of its ownK063578 Promos Modular Shoulder SystemPlus Orthopedics AG · 2007 · Recalled
- Descendant · 3 generations on · 52 of its ownK081016 Smith & Nephew, Inc., Promos Reverse Shoulder SystemSmith & Nephew, Inc. · 2008 · Recalled
- Descendant · 4 generations on · 44 of its ownK110598 SMR Reverse Shoulder SystemLima Corporate S.P.A. · 2011 · Recalled
Showing 5 of 135 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 135 · See all- K032126Promos ShoulderPlus Orthopedics · 2004 · cites it directly130descendants
- K042021Exactech Equinoxe Shoulder SystemExactech, Inc. · 2004 · cites it directly71descendants
- K063578Promos Modular Shoulder SystemPlus Orthopedics AG · 2007 · 2 generations on67descendants
- K081016Smith & Nephew, Inc., Promos Reverse Shoulder SystemSmith & Nephew, Inc. · 2008 · 3 generations on52descendants
- K110598SMR Reverse Shoulder SystemLima Corporate S.P.A. · 2011 · 4 generations on44descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| 0 (this device) | K990136 | Anatomica Glenoid Component | Sulzer Orthopedics, Inc. | 1999 | — |
| +1 | K032126 | Promos Shoulder | Plus Orthopedics | 2004 | — |
| +1 | K042021 | Exactech Equinoxe Shoulder System | Exactech, Inc. | 2004 | 10 |
| +2 | K063578 | Promos Modular Shoulder System | Plus Orthopedics AG | 2007 | 4 |
| +3 | K081016 | Smith & Nephew, Inc., Promos Reverse Shoulder System | Smith & Nephew, Inc. | 2008 | 2 |
| +4 | K110598 | SMR Reverse Shoulder System | Lima Corporate S.P.A. | 2011 | 1 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2004 | 2 | 0 |
| 2005 | 1 | 0 |
| 2006 | 2 | 0 |
| 2007 | 1 | 0 |
| 2008 | 1 | 0 |
| 2010 | 8 | 0 |
| 2011 | 9 | 0 |
| 2012 | 8 | 0 |
| 2013 | 6 | 0 |
| 2014 | 5 | 0 |
| 2015 | 6 | 0 |
| 2016 | 6 | 0 |
| 2017 | 5 | 0 |
| 2018 | 10 | 0 |
| 2019 | 8 | 0 |
| 2020 | 4 | 0 |
| 2021 | 8 | 0 |
| 2022 | 9 | 0 |
| 2023 | 10 | 0 |
| 2024 | 8 | 0 |
| 2025 | 10 | 0 |
| 2026 | 8 | 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? (7)
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 |
|---|---|---|---|
| * | — | Sulzer Orthopedics Select Shoulder Curved Back Pegged Glenoid Named without a submission number | |
| * | — | Orthomet/3M Modular Neer II Shoulder System Named without a submission number | |
| * | — | Zimmer Fenlin Total Shoulder Named without a submission number | |
| * | — | Smith & Nephew Richards Cofield Shoulder Named without a submission number | |
| * | — | Kirschner/Biomet Atlas Shoulder Named without a submission number | |
| * | — | Biomet Bio-Modular Total Shoulder Named without a submission number | |
| * | — | Depuy Global Total Shoulder System Named without a submission number |
What descends from it? (135)
See all 1354 later devices cite it directly; ranked here by how many devices descend from each in turn.
Has anything in its family been recalled? (0 Class I)
Recalls of this device
| Date | Class | Recall | Root cause | Reason |
|---|---|---|---|---|
| Sep 4, 2012 | Class II | Z-0226-2013 | Error in labeling | Zimmer Inc., is initiating a correction to the patient labels of products manufactured before March 20I0 by the Zimmer GmbH production site in Winterthur, Switzerland, after receiving four complaints of a discrepancy between product… |
| Jun 25, 2007 | Not classified | Z-1194-2007 | Other | The package actually contains a knee patellar implant. |
No ancestor or descendant has a Class I recall.
What does this lineage say?
- Of its descendants, K032126 (Plus Orthopedics, 2004) has gone furthest, with 130 descendants of its own.
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?
The Anatomica All-Poly Glenoid component is intended for cemented use in treatment of the following:
1. Advanced wear and tear of the shoulder joint resulting from degenerative, posttraumatic or rheumatoid arthritis.
Omarthrosis.
Rheumatoid arthritis.
Revision of shoulder prosthesis.
Traumatology: the only cone to be used in traumatological indications is the traumatology cone.
Indications for use read by OCR from a scanned FDA summary, so letters may be misread. Check the PDF before quoting it.
https://510kreport.com/device/K990136 · printed Nov 6, 2026
Cite this page
510(k) Report. “K990136: Anatomica Glenoid Component.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K990136
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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