510(k) Report

510(k) · Cleared

Cleared

Smith & Nephew RF Cannulae

K063467510(k) SpecialCleared Nov 21, 200628-day reviewClass II21 CFR 882.4725

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

Smith & Nephew, Inc. · GXI Probe, Radiofrequency Lesion

Cleared on Nov 21, 2006 as substantially equivalent to K034012 (Smith & Nephew, Inc., 2004) after a 28-day review. Its family tree reaches back 4 generations to 1987. 2 later devices descend from it.

Decided
Nov 21, 2006
Review
28 days
Class
Class II
Product code
GXI
Recalls
None
Predicates
1

Its longest line of descent runs back 4 generations to K870028 (1987). 2 later devices descend from it, 1 citing it directly.

  1. Root · 4 generations backK870028 SMK Sluyter-Mehta Cannulae, RF Pole, Pole,FlexibleRadionics, Inc. · 1987
  2. 3 generations backK963577 Radionics Sluijter-Mehta CannulaRadionics, Inc. · 1996
  3. 2 generations backK980430 Radionics Disposable RF Cannulae (SC-C, RFK-DB, RFK-DS)Radionics, Inc. · 1998
  4. 1 generation backK034012 Smith & Nephew RF Denervation Probes & RF CannulaeSmith & Nephew, Inc. · 2004 · Recalled
  5. This deviceK063467 Smith & Nephew RF CannulaeSmith & Nephew, Inc. · 2006
  6. Descendant · cites it directly · 1 of its ownK090955 Smith & Nephew RF CannulateSmith & Nephew, Inc. · 2009 · Recalled
  7. Descendant · 2 generations on · 0 of its ownK253907 Disposable Radiofrequency CannulaAbbott Medical · 2026

Most influential descendants

Showing 2 of 2 · See all
  • K090955Smith & Nephew RF CannulateSmith & Nephew, Inc. · 2009 · cites it directly1descendant
  • K253907Disposable Radiofrequency CannulaAbbott Medical · 2026 · 2 generations on0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−4K870028SMK Sluyter-Mehta Cannulae, RF Pole, Pole,FlexibleRadionics, Inc.1987—
−3K963577Radionics Sluijter-Mehta CannulaRadionics, Inc.1996—
−2K980430Radionics Disposable RF Cannulae (SC-C, RFK-DB, RFK-DS)Radionics, Inc.1998—
−1K034012Smith & Nephew RF Denervation Probes & RF CannulaeSmith & Nephew, Inc.20043
0 (this device)K063467Smith & Nephew RF CannulaeSmith & Nephew, Inc.2006—
+1K090955Smith & Nephew RF CannulateSmith & Nephew, Inc.20091
+2K253907Disposable Radiofrequency CannulaAbbott Medical2026—

Descendants by year cleared

Year clearedDevicesWith a Class I recall
200910
202610
FIG. 1 — Lineage of K063467, 1987–2026Source: FDA 510(k) summaries, read by 510(k) Report · How lineage is built

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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 GXI? 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 GXI device

  1. #1 K253907 Disposable Radiofrequency Cannulascore 12.7 · 6 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K034012Smith & Nephew RF Denervation Probes & RF Cannulae
Summary page 1
…Fundamental Scientific Technology to the following legally marketed device in commercial distribution: Smith & Nephew RF Probe and Cannulae (K034012). E. Description of Device The Smith & Nephew RF Denervation Probe is a temperature sensing elect…
Smith & Nephew, Inc.20043

Also cleared against K034012: 3 other devices →

What descends from it? (2)

1 later device cites it directly; ranked here by how many devices descend from each in turn.

NumberDeviceApplicantDecidedDescendants
K090955Smith & Nephew RF CannulateSmith & Nephew, Inc.20091

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 19 years and passes through 2 companies; a new generation was cleared every 6.0 years on median.
  • 1 of the 4 ancestors has a recall of any class.
  • Of its descendants, K090955 (Smith & Nephew, Inc., 2009) has gone furthest, with 1 descendant of its own.
  • 3 other devices also cite its predicate K034012.

How does its category compare?

All GXI devices

GXI Probe, Radiofrequency Lesion: FDA decisions, review times, recalls and adverse event reports over 20 years.

FDA decisions per year · GXI

4in 2025

2007: 42008: 22009: 22010: 22011: 32012: 12013: 12014: 12015: 12016: 32017: 32018: 12019: 32020: 32022: 22025: 42026 (partial year): 2
2007high 4 (2007) · low 0 (2021)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · GXI

183in 2025

2007: 87 days median2011: 64 days median2016: 240 days median2017: 125 days median2019: 63 days median2020: 255 days median2025: 183 days median
2007high 255 (2020) · low 63 (2019)2026

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

Recalls per year · GXI

1in 2019

2007: 32008: 12010: 12012: 12013: 12017: 12019: 12026 (partial year): 3
2007high 3 (2007) · low 0 (2009)2026

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

Adverse event reports per year · GXI

98in 2025

2007: 12008: 42009: 102010: 82011: 52012: 142013: 252014: 202015: 232016: 162017: 1502018: 1472019: 932020: 312021: 302022: 462023: 352024: 452025: 98
2007high 150 (2017) · low 1 (2007)2025

MAUDE reports naming product code GXI, 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
200748731
20082—14
20092—010
20102—18
201136405
20121—114
20131—125
20141—020
20151—023
20163240016
201731251150
20181—0147
2019363193
20203255031
20210—030
20222—046
20230—035
20240—045
20254183098
20262—3—

What is it indicated for?

Smith & Nephew RF Cannulae are intended to facilitate placement of Smith & Nephew RF Denervation Probes. The Smith & Nephew RF Cannulae are indicated for use in RF heat lesion procedures for the relief of pain.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K063467: Smith & Nephew RF Cannulae.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 4, 2026. https://510kreport.com/device/K063467

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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