510(k) Report

510(k) · Cleared

Cleared

Ultra Low Profile Rongeur

K062711510(k) TraditionalCleared Mar 7, 2007177-day reviewClass II21 CFR 882.4840

Data to Oct 25, 2026 (FDA decisions) Oct 12, 2026 (recalls) Sep 30, 2026 (MAUDE) refreshed weekly, last Nov 3, 2026

Baxano, Inc. · HAE Rongeur, Manual

Cleared on Mar 7, 2007 after a 177-day review. The FDA summary names its predicate without a number. 18 later devices descend from it.

Decided
Mar 7, 2007
Review
177 days
Class
Class II
Product code
HAE
Recalls
None
Predicates
0

18 later devices descend from it, 2 citing it directly.

Descendants, by year cleared 2010: 1 descendant cleared2008: 1 descendant cleared2016: 1 descendant cleared2013: 1 descendant cleared2018: 1 descendant cleared2012: 1 descendant cleared2021: 1 descendant cleared2024: 2 descendants cleared2022: 1 descendant cleared2019: 1 descendant cleared2025: 3 descendants cleared2026: 4 descendants cleared20052010201520202025
  1. This deviceK062711 Ultra Low Profile RongeurBaxano, Inc. · 2007
  2. Descendant · cites it directly · 13 of its ownK093062 Vertos Medical Mild Device KitX-Sten Corp. · 2010
  3. Descendant · 2 generations on · 7 of its ownK180876 DTRAX Spinal SystemProvidence Medical Technology, Inc. · 2018
  4. Descendant · 3 generations on · 6 of its ownK190201 CORUS Spinal SystemProvidence Medical Technology, Inc. · 2019
  5. Descendant · 2 generations on · 5 of its ownK212636 CORUS Spinal System-XProvidence Medical Technology, Inc. · 2021
  6. Descendant · 3 generations on · 4 of its ownK240625 CORUS Navigation Access SystemProvidence Medical Technology, Inc. · 2024

Showing 5 of 18 descendants. See all descendants

Descendants cleared per year

2008: 12010: 12012: 12013: 12016: 12018: 12019: 12021: 12022: 12024: 22025: 32026: 4
2008high 4 (2026) · low 0 (2009)2026

Most influential descendants

Showing 5 of 18 · See all
  • K093062Vertos Medical Mild Device KitX-Sten Corp. · 2010 · cites it directly13descendants
  • K180876DTRAX Spinal SystemProvidence Medical Technology, Inc. · 2018 · 2 generations on7descendants
  • K190201CORUS Spinal SystemProvidence Medical Technology, Inc. · 2019 · 3 generations on6descendants
  • K212636CORUS Spinal System-XProvidence Medical Technology, Inc. · 2021 · 2 generations on5descendants
  • K240625CORUS Navigation Access SystemProvidence Medical Technology, Inc. · 2024 · 3 generations on4descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
0 (this device)K062711Ultra Low Profile RongeurBaxano, Inc.2007—
+1K093062Vertos Medical Mild Device KitX-Sten Corp.2010—
+2K180876DTRAX Spinal SystemProvidence Medical Technology, Inc.2018—
+3K190201CORUS Spinal SystemProvidence Medical Technology, Inc.2019—
+2K212636CORUS Spinal System-XProvidence Medical Technology, Inc.2021—
+3K240625CORUS Navigation Access SystemProvidence Medical Technology, Inc.2024—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200810
201010
201210
201310
201610
201810
201910
202110
202210
202420
202530
202640
FIG. 1 — Lineage of K062711, 2007–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

Get the monthly Device Review Tracker

Notable FDA decisions, review times and new Class I recalls. See an issue.

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. #1 K260446 Tontarra Punches and Rongeursscore 12.6 · 3 generations · no Class I recall
  2. #2 Held for the reportin the report
  3. #3 Held for the reportin the report
Get a 510(k) Report

What was it cleared against? (5)

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.

TypeNumberDeviceApplicantDecidedRecalls
*—Codman Laminectomy Shaver
Named without a submission number
—
*—Integra Ruggles Instrument
Named without a submission number
—
*—US Surgical Kerrison Spinal Rongeur
Named without a submission number
—
*—Zeppelin Laminectomy Rongeur
Named without a submission number
—
*—Bilman Disc FX System
Named without a submission number
—

What descends from it? (18)

See all 18

2 later devices cite it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K093062Vertos Medical Mild Device KitX-Sten Corp.201013
K081651Instrumed RongeurInstrumed International, Inc.20083

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?

  • Of its descendants, K093062 (X-Sten Corp., 2010) has gone furthest, with 13 descendants of its own.

How does its category compare?

All HAE devices

HAE Rongeur, Manual: FDA decisions, review times, recalls and adverse event reports over 20 years. 2007, this device’s year, is highlighted.

FDA decisions per year · HAE

1in 2025

2007: 22008: 22010: 22012: 22013: 22015: 12016: 42018: 12020: 22021: 12022: 22023: 22025: 12026 (partial year): 1
2007high 4 (2016) · low 0 (2009)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · HAE

270in 2016

2016: 270 days median
2007high 270 (2016)2026

Receipt to decision; years with fewer than 3 clearances left blank.

Recalls per year · HAE

2in 2023

2023: 2
2007high 2 (2023) · low 0 (2007)2026

Class I (0 since 2007) Class II/III not classified

Adverse event reports per year · HAE

10in 2025

2007: 42008: 52009: 62010: 102011: 312012: 472013: 202014: 152015: 252016: 342017: 252018: 292019: 242020: 252021: 122022: 132023: 102024: 92025: 10
2007high 47 (2012) · low 4 (2007)2025

MAUDE reports naming product code HAE, not matched to any one device; reports are not rates.

View these four charts as a table
YearDecisionsMedian 510(k) review, daysRecalls (Class I)MAUDE reports
20072—04
20082—05
20090—06
20102—010
20110—031
20122—047
20132—020
20140—015
20151—025
20164270034
20170—025
20181—029
20190—024
20202—025
20211—012
20222—013
20232—210
20240—09
20251—010
20261—0—

What is it indicated for?

The Baxano, Inc. Ultra Low Profile Rongeur is designed for accessing, cutting, and biting soft tissue and bone during surgery involving the spinal column.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K062711: Ultra Low Profile Rongeur.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K062711

Report an extraction error

Tell us what is wrong; we check it against the FDA summary.

Are you the manufacturer?

Send a correction or an update to this page, for example a newer model or a public statement about a recall.

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