Leksell Stereotactic System Neurosurgical Instruments

Disposable Biopsy Needle AND Aspiration Tube

Registry build 21.09.26
5manufacturers in China registered for this device type
58catalogue numbers in this listing
16510(k) clearances naming this product code
4recalls on this code

Who Else Makes It

Concentrated in Jiangsu (2), Shanghai (1), Shandong (1). 2 of them are registered as contract manufacturers, able to build to a buyer’s own specification.

Chinese manufacturers registered for FDA product code HAW
Manufacturer City Province Registered as Device types
Paragon Medical Device (Changzhou) Co., Ltd. Changzhou Jiangsu Contract manufacturer 53
Shandong Weigao Orthopaedic Device Co., Ltd. Weihai Shandong Contract manufacturer 42
Zimmer (Shanghai) Medical International Trading Co., Ltd. Shanghai Shanghai Exporter 106
Medtronic (Changzhou) Medical Devices Technology Co., Ltd. Changzhou Jiangsu Manufacturer 53
Sinovation (Beijing) Medical Technology Co., Ltd. Beijing Beijing Manufacturer 1

Record

Regulatory record for Leksell Stereotactic System Neurosurgical Instruments
Listed by Elekta Instrument AB, Sweden
FDA product code HAW
Device type Neurological Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
510(k) K152558
Record published 2016-09-24
Record revised 2025-12-15 (version 5)

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Moist Heat or Steam Sterilization
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Supplied as a kit Yes
Label carries lot or batch number, expiry date
Sizes Outer diameter 0.9 to 4 mm; length 70 to 190 mm
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for Leksell Stereotactic System Neurosurgical Instruments
Catalogue number Size Status
60377-01 In distribution
50398-01 Outer Diameter 1.5 mm In distribution
1024404 Outer Diameter 1.9 mm In distribution
50378-01 Inner Diameter In distribution
1522153 In distribution
60080-60 Inner diameter In distribution
911934 In distribution
A2800-15 In distribution
1506444 In distribution
1018428 Outer Diameter 1.5 mm In distribution
60377-02 Outer Diameter 3.2 mm In distribution
912465 In distribution
A2430-01 In distribution
1024398 Outer Diameter 2.6 mm In distribution
911933 In distribution
911761 In distribution
1018425 Outer Diameter 2.1 mm In distribution
A2800-26 In distribution
A2200-01 In distribution
1018439 Outer Diameter 2.1 mm In distribution
1018449 Outer Diameter 1.5 mm In distribution
1505535 Inner diameter In distribution
60080-35 Inner diameter In distribution
60081-21 Inner diameter In distribution
1075647 In distribution
1020176 Outer Diameter 0.9 mm In distribution
60380-01 In distribution
60080-32 Inner diameter In distribution
60080-40 Inner diameter In distribution
307165 Length 190.0 mm In distribution
60081-60 Inner diameter In distribution
1018446 Outer Diameter 2.1 mm In distribution
907801 Length 190.0 mm In distribution
60081-40 Inner diameter In distribution
A2600-01 In distribution
1524113 Outer Diameter 3.2 mm In distribution
14001050 In distribution
1018452 Outer Diameter 0.9 mm In distribution
60080-21 Inner diameter In distribution
60379-01 Outer Diameter 4.0 mm In distribution
1524112 Outer Diameter 2.1 mm In distribution
1020177 In distribution
1018442 Outer Diameter 1.6 mm In distribution
1505536 Inner diameter In distribution
50376-01 In distribution
60080-25 Inner diameter In distribution
50378-02 Inner Diameter In distribution
50386-01 In distribution
1018432 Biopsy length In distribution
50389-01 In distribution
1024401 Outer Diameter 3.5 mm In distribution
60081-25 Inner diameter In distribution
60379-02 Outer Diameter 4.0 mm In distribution
1018435 Biopsy length In distribution
1522155 In distribution
1020173 Outer Diameter 1.5 mm In distribution
60081-35 Inner diameter In distribution
60081-32 Inner diameter In distribution

Same Product Code

Other products under the same FDA product code
Product Sold by Catalogue numbers
Neurological Stereotaxic Instrument Medtronic Navigation, Inc. 844
PMT Corporation – Stereotactic PMT Corp. 255
Leksell Stereotactic System Elekta Instrument AB 199
Neurological Stereotaxic Instrument Inomed Medizintechnik Gmbh 146
Neurological Stereotaxic Instrument Stryker Leibinger Gmbh & Co. KG 125
Geniant Cranial KOH Young Technology Inc. 113
CRW® Integra Lifesciences Corporation 107
Leksell Stereotactic System Elekta Solutions AB 93
microTargeting™ Insertion Tube with Stylet FHC, Inc. 60
Leksell Vantage Stereotactic System Elekta Instrument AB 53
Stealth Autoguide™ System Medtronic Navigation, Inc. 50
microTargeting™ Insertion Tube FHC, Inc. 48

Showing 12 of 1,137. All products under Neurological Stereotaxic Instrument

510(K) Clearances

FDA 510(k) clearances naming this product code
Clearance Decision date
K190887 2019-08-01
K171123 2017-09-15
K152558 2016-03-02
K080355 2009-05-01
K080250 2008-05-13
K051746 2005-07-25
K040979 2004-07-23
K033340 2004-02-12
K031999 2003-07-25
K031980 2003-07-25
K013861 2001-12-06
K992882 1999-09-24
K991636 1999-07-20
K973684 1998-03-31
K972324 1998-03-02
K961639 1996-07-26

Recalls Naming This Product

3 recalls name this product by its own identifiers, the 510(k) it is cleared under.

Recalls naming the identifiers of Leksell Stereotactic System Neurosurgical Instruments
Recalled by Identified by Initiated FDA class Root cause Reason Quantity
Elekta Instrument AB 510(k) number 2024-09-25 Class I Under Investigation by firm Elekta has become aware that Disposable Biopsy Needles can contain some microscopic debris on the inside of the biopsy needle. The material in the debris is stainless steel, same material as the biopsy needle. No debris has been found on th 111 kits (666 needles)
Elekta Instrument AB 510(k) number 2024-03-15 Class I Under Investigation by firm Elekta has become aware that Disposable Biopsy Needles (911933) from one batch (837838839) can contain some microscopic debris on the inside of the biopsy needle. The material in the debris is stainless steel, same material as the biopsy ne 601 needles
Elekta Instrument AB 510(k) number 2023-03-01 Class II Labeling Change Control The incorrect IFU was distributed with the devices. 70 devices

Recalls

1 of these is Class II. Class II means a temporary or reversible health consequence. Volume alone is not a quality signal: a manufacturer that ships more recalls more.

Recalls referencing this product code
Initiated FDA class Root cause Reason Quantity Closed
2020-06-10 Class II Device Design The locking mechanism at the interface of the Instrument Carrier and the Leksell Vantage Arc may not function properly. 51 devices 2024-08-27

Source: U.S. FDA establishment registration and device listing records, public domain. Restructured for clarity and searchability. Not affiliated with or endorsed by the FDA. Records are records: nothing here is an offer of sale.

Where China Actually Supplies

Every device page names the company that lists it and the factories registered to make the same thing. These are the sections with the most of them.

5,100manufacturers registered in China
2,581device types they are registered for
340,248device records, each naming its maker
31provinces with a registered manufacturer