510(k) Report

510(k) · Cleared

Cleared

Contiplex D Continuous Nerve Block Set, Model 331687, 331686, 331685, 331680

K100241510(k) TraditionalCleared Apr 16, 201079-day reviewClass II21 CFR 868.5150

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

B.Braun Medical, Inc. · BSP Needle, Conduction, Anesthetic (W/Wo Introducer)

Cleared on Apr 16, 2010 as substantially equivalent to K090995 (B.Braun Medical, Inc., 2009) and 1 other predicate after a 79-day review. Its family tree reaches back 6 generations to 1984. 1 of the 21 devices in its family, counting itself, has a Class I recall. 7 later devices descend from it.

Decided
Apr 16, 2010
Review
79 days
Class
Class II
Product code
BSP
Recalls
None
Predicates
2

Its longest line of descent runs back 6 generations to K840287 (1984). 13 ancestors in all, the oldest K801912 (1980). 7 later devices descend from it, 3 citing it directly. 1 of the 21 devices in this family, counting this one, has a Class I recall.

Other ancestors, by year clearedDescendants, by year cleared 2007: 1 other ancestor2000: 2 other ancestors2003: 1 other ancestor2002: 1 other ancestor1983: 1 other ancestor1980: 1 other ancestor, 1 with a Class I recall12020: 2 descendants cleared2012: 1 descendant cleared2018: 1 descendant cleared2016: 1 descendant cleared2022: 1 descendant cleared2024: 1 descendant clearedK840287 · Brachial Plexus Anesthesia Tray · Burron Medical Products, Inc. · 1984K013041 · Plexolong Sets · Pajunk GmbH · 2002K023218 · Modification to Plexolong Sets · Pajunk GmbH · 2003K033018 · Stimulong Plus Catheter Set Model, Various · Pajunk GmbH · 2004K063282 · Contiplex Stim Continuous Nerve Block Set · B.Braun Medical, Inc. · 2007K090995 · B. Braun Contiplex Continuous Nerve Block Set · B.Braun Medical, Inc. · 200919801990200020102020
Other ancestors, by generationDescendants, by generation 1 generation back: 1 other ancestor2 generations back: 1 other ancestor3 generations back: 1 other ancestor4 generations back: 2 other ancestors5 generations back: 2 other ancestors, 1 with a Class I recall1 1 generation forward: 3 descendants2 generations forward: 3 descendants3 generations forward: 1 descendant K090995 · B. Braun Contiplex Continuous Nerve Block Set · B.Braun Medical, Inc. · 2009K063282 · Contiplex Stim Continuous Nerve Block Set · B.Braun Medical, Inc. · 2007K033018 · Stimulong Plus Catheter Set Model, Various · Pajunk GmbH · 2004K023218 · Modification to Plexolong Sets · Pajunk GmbH · 2003K013041 · Plexolong Sets · Pajunk GmbH · 2002K840287 · Brachial Plexus Anesthesia Tray · Burron Medical Products, Inc. · 1984−50
  1. Root · 6 generations backK840287 Brachial Plexus Anesthesia TrayBurron Medical Products, Inc. · 1984
  2. 5 generations backK013041 Plexolong SetsPajunk GmbH · 2002
  3. 4 generations backK023218 Modification to Plexolong SetsPajunk GmbH · 2003
  4. 3 generations backK033018 Stimulong Plus Catheter Set Model, VariousPajunk GmbH · 2004
  5. 2 generations backK063282 Contiplex Stim Continuous Nerve Block SetB.Braun Medical, Inc. · 2007
  6. 1 generation backK090995 B. Braun Contiplex Continuous Nerve Block SetB.Braun Medical, Inc. · 2009
  7. This deviceK100241 Contiplex D Continuous Nerve Block Set, Model 331687, 331686…B.Braun Medical, Inc. · 2010
  8. Descendant · cites it directly · 2 of its ownK173763 iovera systemMyoscience, Inc. · 2018
  9. Descendant · cites it directly · 2 of its ownK121846 Contiplex C Continuous Peripheral Nerve Block NeedleB.Braun Medical, Inc. · 2012
  10. Descendant · 2 generations on · 1 of its ownK220656 iovera SystemPacira Biosciences, Inc. · 2022
  11. Descendant · 3 generations on · 0 of its ownK243677 iovera° SystemPacira Biosciences, Inc. · 2024
  12. Descendant · cites it directly · 0 of its ownK192914 Stimuplex Onvision SystemPhilips Medical Systems Nederland B.V. · 2020

Showing 5 of 7 descendants. See all descendants

Descendants cleared per year

2012: 12016: 12018: 12020: 22022: 12024: 1
2012high 2 (2020) · low 0 (2013)2026

Class I recalls in this family

Most influential descendants

Showing 5 of 7 · See all
  • K173763iovera systemMyoscience, Inc. · 2018 · cites it directly2descendants
  • K121846Contiplex C Continuous Peripheral Nerve Block NeedleB.Braun Medical, Inc. · 2012 · cites it directly2descendants
  • K220656iovera SystemPacira Biosciences, Inc. · 2022 · 2 generations on1descendant
  • K243677iovera° SystemPacira Biosciences, Inc. · 2024 · 3 generations on0descendants
  • K192914Stimuplex Onvision SystemPhilips Medical Systems Nederland B.V. · 2020 · cites it directly0descendants
View FIG. 1 as a table

Line of descent and top descendants

GenerationNumberDeviceApplicantDecidedRecalls
−6K840287Brachial Plexus Anesthesia TrayBurron Medical Products, Inc.1984—
−5K013041Plexolong SetsPajunk GmbH2002—
−4K023218Modification to Plexolong SetsPajunk GmbH2003—
−3K033018Stimulong Plus Catheter Set Model, VariousPajunk GmbH2004—
−2K063282Contiplex Stim Continuous Nerve Block SetB.Braun Medical, Inc.2007—
−1K090995B. Braun Contiplex Continuous Nerve Block SetB.Braun Medical, Inc.2009—
0 (this device)K100241Contiplex D Continuous Nerve Block Set, Model 331687, 331686, 331685, 331680B.Braun Medical, Inc.2010—
+1K173763iovera systemMyoscience, Inc.2018—
+1K121846Contiplex C Continuous Peripheral Nerve Block NeedleB.Braun Medical, Inc.2012—
+2K220656iovera SystemPacira Biosciences, Inc.2022—
+3K243677iovera° SystemPacira Biosciences, Inc.2024—
+1K192914Stimuplex Onvision SystemPhilips Medical Systems Nederland B.V.2020—

Other ancestors by year cleared

Year clearedDevicesWith a Class I recall
198011
198310
200020
200210
200310
200710

Descendants by year cleared

Year clearedDevicesWith a Class I recall
201210
201610
201810
202020
202210
202410
FIG. 1 — Lineage of K100241, 1984–2024Source: 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.

1 device in this family has a Class I recall. 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 BSP device

  1. #1 K241954 SonoBlock; SonoBlock IIscore 11.0 · 1 generation · 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? (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.

TypeNumberDeviceApplicantDecidedRecalls
*K090995B. Braun Contiplex Continuous Nerve Block Set
Summary page 1
…Class II, Product Code BSP 868.5150 PREDICATE DEVICES: Contiplex® Continuous Nerve Block Set, B. Braun Medical, Inc., 1K090995. Class II, CAZ, 868.5140 (containing Contiplex Tuohy and Straight Needle components, Class II, B…
B.Braun Medical, Inc.2009—
*K063380Echostim Facet Tip
Summary page 1
…tiplex Tuohy and Straight Needle components, Class II, BSP 868.5150) EchoStim® Facet Tip, Navel, Inc., K063380, Class IL, BSP, 868.5150 DESCRIPTION: The Contiplex® D Insulated Needles a…
Havel'S, Inc.2007—

Also cleared against K090995: 1 other device →

What descends from it? (7)

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

NumberDeviceApplicantDecidedDescendants
K173763iovera systemMyoscience, Inc.20182
K121846Contiplex C Continuous Peripheral Nerve Block NeedleB.Braun Medical, Inc.20122
K192914Stimuplex Onvision SystemPhilips Medical Systems Nederland B.V.20200

Has anything in its family been recalled? (1 Class I)

No FDA recall names this device.

Relatives with a Class I recall

Class I is FDA’s most serious recall class. A recall in the family tree is context for this device, not evidence about it.

  • K801912Arrow Positive Placement Con/Epidural anArrow Intl., Inc. · 1980 · 5 generations back · ◆ in the 1980 ancestors bar of FIG. 11 Class I recall

What does this lineage say?

  • The line of descent spans 26 years and passes through 3 companies; a new generation was cleared every 2.2 years on median.
  • 3 of the 13 ancestors have a recall of any class; 1 has a Class I recall.
  • Of its descendants, K173763 (Myoscience, Inc., 2018) has gone furthest, with 2 descendants of its own.
  • 1 other device also cites its predicate K090995.

How does its category compare?

All BSP devices

BSP Needle, Conduction, Anesthetic (W/Wo Introducer): FDA decisions, review times, recalls and adverse event reports over 20 years. 2010, this device’s year, is highlighted.

FDA decisions per year · BSP

4in 2025

2007: 32008: 82009: 52010: 32011: 32012: 32013: 22014: 22015: 22016: 62017: 42018: 82019: 22020: 32021: 32022: 22024: 32025: 4
2007high 8 (2008) · low 0 (2023)2026

2026 to Oct 25, outlined.

Median 510(k) review, days · BSP

170in 2025

2007: 189 days median2008: 127 days median2009: 97 days median2010: 79 days median2011: 114 days median2012: 148 days median2016: 268 days median2017: 186 days median2018: 241 days median2020: 269 days median2021: 265 days median2024: 70 days median2025: 170 days median
2007high 269 (2020) · low 70 (2024)2026

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

Recalls per year · BSP

1in 2020

2016: 12019: 12020: 12026 (partial year): 1, 1 Class I
2007high 1 (2016) · low 0 (2007)2026

Class I (1 since 2007) Class II/III not classified

Adverse event reports per year · BSP

86in 2025

2007: 262008: 242009: 302010: 492011: 332012: 202013: 322014: 412015: 382016: 1522017: 342018: 692019: 862020: 782021: 522022: 842023: 752024: 662025: 86
2007high 152 (2016) · low 20 (2012)2025

MAUDE reports naming product code BSP, 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
20073189026
20088127024
2009597030
2010379049
20113114033
20123148020
20132—032
20142—041
20152—038
201662681152
20174186034
20188241069
20192—186
20203269178
20213265052
20222—084
20230—075
2024370066
20254170086
20260—1 (1)—

What is it indicated for?

The B. Braun Stimuplex® D Plus Insulated Echogenic Needle is intended for use in regional anesthesia and pain therapy to target peripheral nerves by transferring electrical impulses from a nerve stimulator and for visualization of an echogenic reflective pattern at the needle tip using an ultrasound imaging device. The needle is used to inject a single dose of local anesthetic or analgesic to the targeted nerve bundle for general and orthopedic surgery.…

Read the full statement (238 words)

The B. Braun Stimuplex® D Plus Insulated Echogenic Needle is intended for use in regional anesthesia and pain therapy to target peripheral nerves by transferring electrical impulses from a nerve stimulator and for visualization of an echogenic reflective pattern at the needle tip using an ultrasound imaging device. The needle is used to inject a single dose of local anesthetic or analgesic to the targeted nerve bundle for general and orthopedic surgery.

The B. Braun Stimuplex® D Insulated Needle is intended for use in regional anesthesia and pain therapy to locate by stimulation peripheral nerves by transferring electrical impulses from a nerve stimulator. The needle is used to inject a single dose of local anesthetic or analgesic to the targeted nerve bundle for general and orthopedic surgery.

The B. Braun Contiplex® D Insulated Needle is intended for use in regional anesthesia and pain therapy to locate, by stimulation, peripheral nerves by transferring electrical impulses from a nerve stimulator. The needle is used to inject and facilitate the continuous administration of local anesthetics or analgesics to the targeted nerve bundle for general and orthopedic surgery.

The Contiplex D Continuous Nerve Block Set is intended to provide continuous and/or intermittent infusion of local anesthetics and analgesics for peripheral plexus anesthesia and pain management during the pre-operative, perioperative and post-operative periods associated with general and orthopedic surgery. The Contiplex D polyamide indwelling catheter may remain indwelling for up to 72 hours.

Indications for use as stated in the FDA summary.

Cite this page

510(k) Report. “K100241: Contiplex D Continuous Nerve Block Set, Model 331687, 331686, 331685, 331680.” Lineage record from FDA 510(k) data and the FDA summary. Updated Nov 3, 2026. Accessed Nov 6, 2026. https://510kreport.com/device/K100241

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