510(k) · Cleared
ClearedSymmetry Kerrison Disposable Tip Rongeurs
Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly
Symmetry Surgical · HAE Rongeur, Manual
Cleared on Aug 5, 2013 as substantially equivalent to K092227 (Integra Lifesciences Corp., 2010) after a 157-day review. Its family tree reaches back 2 generations to 1990. 1 later device descends from it.
- Decided
- Aug 5, 2013
- Review
- 157 days
- Class
- Class II
- Product code
- HAE
- Recalls
- None
- Predicates
- 1
Its longest line of descent runs back 2 generations to K902819 (1990). 3 ancestors in all. 1 later device descends from it, 1 citing it directly.
- Root · 2 generations backK902819 Laminectomy RogeurRuggles Corp. · 1990
- 1 generation backK092227 Jarit, Ruggles, R&B Redmond/ Redmond, Miltex, Meisterhand - Kerrison…Integra Lifesciences Corp. · 2010
- This deviceK130541 Symmetry Kerrison Disposable Tip RongeursSymmetry Surgical · 2013
- Descendant · cites it directly · 0 of its ownK161744 Symmetry Sharp Kerrison RongeurSymmetry Surgical, Inc. · 2016
Most influential descendants
Showing 1 of 1 · See all- K161744Symmetry Sharp Kerrison RongeurSymmetry Surgical, Inc. · 2016 · cites it directly0descendants
View FIG. 1 as a table
Line of descent and top descendants
| Generation | Number | Device | Applicant | Decided | Recalls |
|---|---|---|---|---|---|
| −2 | K902819 | Laminectomy Rogeur | Ruggles Corp. | 1990 | — |
| −1 | K092227 | Jarit, Ruggles, R&B Redmond/ Redmond, Miltex, Meisterhand - Kerrison Rongeurs | Integra Lifesciences Corp. | 2010 | — |
| 0 (this device) | K130541 | Symmetry Kerrison Disposable Tip Rongeurs | Symmetry Surgical | 2013 | — |
| +1 | K161744 | Symmetry Sharp Kerrison Rongeur | Symmetry Surgical, Inc. | 2016 | — |
Other ancestors by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 1994 | 1 | 0 |
Descendants by year cleared
| Year cleared | Devices | With a Class I recall |
|---|---|---|
| 2016 | 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 HAE? 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 HAE device
- #1 K260446 Tontarra Punches and Rongeursscore 12.6 · 3 generations · no Class I recall
- #2 Held for the reportin the report
- #3 Held for the reportin the report
What was it cleared against? (2)
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 |
|---|---|---|---|
| * | K092227 | Jarit, Ruggles, R&B Redmond/ Redmond, Miltex, Meisterhand - Kerrison RongeursSummary page 1…e Device: Codman Kerrison Laminectomy Rongeurs, Prea mend me nt Integra Kerrison Rongeurs, K092227, cleared 2/17/10 33… | 2010 |
| * | — | Codman Kerrison Laminectomy Rongeurs Named without a submission number |
What descends from it? (1)
1 later device cites it directly; ranked here by how many devices descend from each in turn.
| Number | Device | Decided | Descendants |
|---|---|---|---|
| K161744 | Symmetry Sharp Kerrison Rongeur | 2016 | 0 |
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 23 years and passes through 3 companies; a new generation was cleared every 19.5 years on median.
- None of the 3 ancestors has a recall.
- Of its descendants, K161744 (Symmetry Surgical, Inc., 2016) has gone furthest, with 0 descendants of its own.
- 5 other devices also cite its predicate K092227.
How does its category compare?
All HAE devicesHAE Rongeur, Manual: FDA decisions, review times, recalls and adverse event reports over 20 years. 2013, this device’s year, is highlighted.
FDA decisions per year · HAE
1in 2025
2026 to Oct 25, outlined.
Median 510(k) review, days · HAE
270in 2016
Receipt to decision; years with fewer than 3 clearances left blank.
Recalls per year · HAE
2in 2023
Class I (0 since 2007) Class II/III not classified
Adverse event reports per year · HAE
10in 2025
MAUDE reports naming product code HAE, 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 | 4 |
| 2008 | 2 | — | 0 | 5 |
| 2009 | 0 | — | 0 | 6 |
| 2010 | 2 | — | 0 | 10 |
| 2011 | 0 | — | 0 | 31 |
| 2012 | 2 | — | 0 | 47 |
| 2013 | 2 | — | 0 | 20 |
| 2014 | 0 | — | 0 | 15 |
| 2015 | 1 | — | 0 | 25 |
| 2016 | 4 | 270 | 0 | 34 |
| 2017 | 0 | — | 0 | 25 |
| 2018 | 1 | — | 0 | 29 |
| 2019 | 0 | — | 0 | 24 |
| 2020 | 2 | — | 0 | 25 |
| 2021 | 1 | — | 0 | 12 |
| 2022 | 2 | — | 0 | 13 |
| 2023 | 2 | — | 2 | 10 |
| 2024 | 0 | — | 0 | 9 |
| 2025 | 1 | — | 0 | 10 |
| 2026 | 1 | — | 0 | — |
What is it indicated for?
The Symmetry Kerrison Disposable Tip Rongeurs are indicated for
cutting bony tissue of the spine.
Indications for use as stated in the FDA summary.
https://510kreport.com/device/K130541 · printed Nov 4, 2026
Cite this page
510(k) Report. “K130541: Symmetry Kerrison Disposable Tip Rongeurs.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K130541
Report an extraction error
Are you the manufacturer?
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