510(k) · Cleared
ClearedLatitude Elbow Prothesis
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Tornier · JDB Prosthesis, Elbow, Semi-Constrained, Cemented
Cleared on Aug 24, 2007 as substantially equivalent to K000003 (Tornier, 2000) and 3 other predicates after a 155-day review. Its family tree reaches back 3 generations to 1989. 6 later devices descend from it.
- Decided
- Aug 24, 2007
- Review
- 155 days
- Class
- Class II
- Product code
- JDB
- Recalls
- None
- Predicates
- 4
Its longest line of descent runs back 3 generations to K883665 (1989). 7 ancestors in all. 6 later devices descend from it, 1 citing it directly.
- Root · 3 generations backK883665 Coonrad Iii Total ElbowZimmer, Inc. · 1989
- 2 generations backK973357 Coonrad/Morrey Total Elbow, New Hinge PinZimmer, Inc. · 1998 · Recalled
- 1 generation backK031218 Modification to Tornier Total Elbow ProsthesisTornier · 2003
- This deviceK070787 Latitude Elbow ProthesisTornier · 2007
- Descendant · cites it directly · 5 of its ownK100562 Latitude Elbow ProsthesisTornier, Inc. · 2010 · Recalled
- Descendant · 2 generations on · 4 of its ownK171010 Latitude EV Total Elbow ArthroplastyTornier, Inc. · 2017
- Descendant · 2 generations on · 1 of its ownK181362 TEMA Elbow SystemLima Corporate S.P.A. · 2019 · Recalled
- Descendant · 2 generations on · 1 of its ownK182461 LATITUDE EV Total Elbow ArthroplastyTornier, Inc. · 2018
- Descendant · 3 generations on · 0 of its ownK222807 TEMA Elbow system - Line extensionLima Corporate S.P.A. · 2022 · Recalled
Showing 5 of 6 descendants. See all descendants
Descendants cleared per year
Most influential descendants
Showing 5 of 6 · See all- K100562Latitude Elbow ProsthesisTornier, Inc. · 2010 · cites it directly5descendants
- K171010Latitude EV Total Elbow ArthroplastyTornier, Inc. · 2017 · 2 generations on4descendants
- K181362TEMA Elbow SystemLima Corporate S.P.A. · 2019 · 2 generations on1descendant
- K182461LATITUDE EV Total Elbow ArthroplastyTornier, Inc. · 2018 · 2 generations on1descendant
- K222807TEMA Elbow system - Line extensionLima Corporate S.P.A. · 2022 · 3 generations on0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −3 | K883665 | Coonrad Iii Total Elbow | Zimmer, Inc. | 1989 | — |
| −2 | K973357 | Coonrad/Morrey Total Elbow, New Hinge Pin | Zimmer, Inc. | 1998 | 1 |
| −1 | K031218 | Modification to Tornier Total Elbow Prosthesis | Tornier | 2003 | — |
| 0 (this device) | K070787 | Latitude Elbow Prothesis | Tornier | 2007 | — |
| +1 | K100562 | Latitude Elbow Prosthesis | Tornier, Inc. | 2010 | 2 |
| +2 | K171010 | Latitude EV Total Elbow Arthroplasty | Tornier, Inc. | 2017 | — |
| +2 | K181362 | TEMA Elbow System | Lima Corporate S.P.A. | 2019 | 1 |
| +2 | K182461 | LATITUDE EV Total Elbow Arthroplasty | Tornier, Inc. | 2018 | — |
| +3 | K222807 | TEMA Elbow system - Line extension | Lima Corporate S.P.A. | 2022 | 1 |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1996 | 1 | 0 |
| 2000 | 1 | 0 |
| 2001 | 1 | 0 |
| 2005 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2010 | 1 | 0 |
| 2017 | 1 | 0 |
| 2018 | 1 | 0 |
| 2019 | 1 | 0 |
| 2020 | 1 | 0 |
| 2022 | 1 | 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 JDB? 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 JDB device
- #1 K222807 TEMA Elbow system - Line extensionscore 4.0 · 7 generations · no Class I recall
- #2 Held for the reportin the report
What was it cleared against? (4)
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 |
|---|---|---|---|
| * | K000003 | Tornier Total Elbow ProsthesisSummary page 1…class: Class II Classification panel: Orthopedic Product code: JDB and JDC 5) Equivalent I Predicate device Tomier Elbow Prosthesis, Torier, K000003, K01 1567, K031218 and K050848 6) Device description Total Elbow replacement is used to treat a number of clinical conditions su… | 2000 |
| * | K011567 | Tornier Total Elbow ProsthesisSummary page 1…Class II Classification panel: Orthopedic Product code: JDB and JDC 5) Equivalent I Predicate device Tomier Elbow Prosthesis, Torier, K000003, K01 1567, K031218 and K050848 6) Device description Total Elbow replacement is used to treat a number of clinical conditions such as seve… | 2001 |
| * | K031218 | Modification to Tornier Total Elbow ProsthesisSummary page 1…Class II Classification panel: Orthopedic Product code: JDB and JDC 5) Equivalent I Predicate device Tomier Elbow Prosthesis, Torier, K000003, K01 1567, K031218 and K050848 6) Device description Total Elbow replacement is used to treat a number of clinical conditions such as severe pain o… | 2003 |
| * | K050848 | Tornier Elbow ProsthesisSummary page 1…ssification panel: Orthopedic Product code: JDB and JDC 5) Equivalent I Predicate device Tomier Elbow Prosthesis, Torier, K000003, K01 1567, K031218 and K050848 6) Device description Total Elbow replacement is used to treat a number of clinical conditions such as severe pain or significan… | 2005 |
What descends from it? (6)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K100562 | Latitude Elbow Prosthesis | 2010 | 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 18 years and passes through 2 companies; a new generation was cleared every 5.2 years on median.
- 1 of the 7 ancestors has a recall of any class.
- Of its descendants, K100562 (Tornier, Inc., 2010) has gone furthest, with 5 descendants of its own.
- 3 other devices also cite its predicate K000003.
How does its category compare?
All JDB devicesJDB Prosthesis, Elbow, Semi-Constrained, Cemented: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.
FDA decisions per year · JDB
1in 2022
2026 to Oct 25, outlined.
Median 510(k) review, days · JDB
Too few JDB 510(k)s in any year since 2007 to give a median.
Recalls per year · JDB
1in 2024
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · JDB
38in 2025
MAUDE reports naming product code JDB, 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 | — | 0 | 3 |
| 2008 | 0 | — | 0 | 13 |
| 2009 | 0 | — | 0 | 10 |
| 2010 | 2 | — | 0 | 7 |
| 2011 | 0 | — | 1 | 6 |
| 2012 | 0 | — | 0 | 6 |
| 2013 | 0 | — | 0 | 2 |
| 2014 | 0 | — | 0 | 5 |
| 2015 | 0 | — | 0 | 44 |
| 2016 | 0 | — | 0 | 11 |
| 2017 | 1 | — | 0 | 26 |
| 2018 | 1 | — | 0 | 39 |
| 2019 | 0 | — | 0 | 31 |
| 2020 | 1 | — | 0 | 32 |
| 2021 | 0 | — | 0 | 23 |
| 2022 | 1 | — | 0 | 58 |
| 2023 | 0 | — | 0 | 29 |
| 2024 | 0 | — | 1 | 163 |
| 2025 | 0 | — | 0 | 38 |
| 2026 | 0 | — | 0 | — |
What is it indicated for?
The Tornier Elbow Prosthesis is intended for total elbow arthroplasty. Prosthetic replacement with this device may be indicated to relieve severe pain or significant disability following the effects of primary or secondary osteoarthtitis and rheumatoid arthritis; correction of fumctional deformities; revision procedures where other treatments or devices have failed; treatment of fractures that are unmanageable using other techniques. The Tornier Elbow Prosthesis is intended for cemented use only.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K070787 · printed Nov 6, 2026
Cite this page
510(k) Report. “K070787: Latitude Elbow Prothesis.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K070787
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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