Microtargeting™ Insertion Tube With Stylet

microTargeting Insertion Tube with Stylet, nonsterile, at target, for use with Nexframe/Nexdrive

Registry build 21.09.26
5manufacturers in China registered for this device type
60catalogue numbers in this listing
6510(k) clearances naming this product code
24recalls 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 microTargeting™ Insertion Tube with Stylet
Listed by FHC, Inc., United States
FDA product code HAW
Device type Neurological Stereotaxic Instrument
Device class Class 2
Regulation 21 CFR 882.4560
Establishment Complaint-file establishment, Manufacturer
510(k) K011775
Record published 2016-09-17
Record revised 2018-07-06 (version 4)

Specifications

Specifications
MRI safety MR Unsafe
Sterilisation Moist Heat or Steam Sterilization, Ethylene Oxide
Supplied sterile Yes
Single use Yes
Prescription Prescription only
Label carries lot or batch number, expiry date
Storage Handling environment humidity 0 to 95 % RH; Storage environment temperature 0 to 40 °C; Storage environment humidity 0 to 95 % RH
Packaging Pk/5 of 5
Sizes Length 74 to 267.85 mm; lumen/inner diameter 0.6 to 1.89 mm; outer diameter 0.9 to 2.12 mm; outer diameter 1.83 m
UDI direct marking Exempt

Catalogue Numbers

Catalogue numbers for microTargeting™ Insertion Tube with Stylet
Catalogue number Size Status
66-IT(ES5)-00531 Outer Diameter 2.12 mm In distribution
66-IT-AR30P-00584 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AR27)-00479 Length 252.85 mm In distribution
66-IT(BP22)-00586 Outer Diameter 1.83 mm In distribution
66-IT-AR27P-00540 Length 252.85 mm In distribution
66-IT(AR32)-00484 Length 257.9 mm In distribution
66-IT(AR35)-00485 Length 203.85 mm In distribution
66-IT(BP16)-00501 Length 175 mm In distribution
66-IT(CV2)-00655 Outer Diameter 2.1 mm In distribution
66-IT(CG7)-00512 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AO9)-00647 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(DB8)-00528 Outer Diameter 1.83 mm In distribution
66-IT(AR31)-00817 Outer Diameter 1.83 mm In distribution
66-IT(BP17)-00502 Outer Diameter 1.83 mm In distribution
66-IT(OC2)-00487 Length 180 mm In distribution
66-IT(AR21)-00474 Length 201.6 mm In distribution
66-IT(DB12)-00521 Lumen/Inner Diameter 1.6 mm In distribution
66-IT-AO6P-00736 Outer Diameter 1.8 mm In distribution
66-IT(AR40)-00499 Outer Diameter 1.83 mm In distribution
66-IT(AR38)-00496 Length 218.85 mm In distribution
66-IT(DB1)-00515 Outer Diameter 1.83 m In distribution
66-IT(AR39)-00497 Length 220 mm In distribution
66-IT(BP11)-00500 Outer Diameter 1.83 mm In distribution
66-IT(DB4)-00524 Outer Diameter 1.83 mm In distribution
66-IT(MD2)-00493 Lumen/Inner Diameter 1.19 mm In distribution
66-IT-AO11P-00867 In distribution
66-IT(AR37)-00495 Length 229.9 mm In distribution
66-IT(CH1)-00673 Outer Diameter 1.8 mm In distribution
66-IT-AR21P-00583 Length 201.6 mm In distribution
66-IT(AO6)-00468 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AR20)-00471 Lumen/Inner Diameter 0.6 mm In distribution
66-IT(BP18)-00503 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AR29)-00866 In distribution
66-IT(FP1)-00526 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(BP20)-00568 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(DB3)-00523 Outer Diameter 1.83 mm In distribution
66-IT(AO10)-00648 Outer Diameter 1.83 mm In distribution
66-IT(DB7)-00527 Length 205.6 mm In distribution
66-IT(AR36)-00494 Length 222 mm In distribution
66-IT(OC1)-00489 Length 175 mm In distribution
66-IT-15P-00821 In distribution
66-IT(DB2)-00522 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(BP2)-00506 Length 179 mm In distribution
66-IT(AR3)-00480 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AR14)-00469 Outer Diameter 1.83 mm In distribution
66-IT(BP8)-00511 Length 219 mm In distribution
66-IT(MD1)-00509 Lumen/Inner Diameter 1.19 mm In distribution
66-IT(BP3)-00507 Outer Diameter 1.83 mm In distribution
66-IT(CV1)-00654 Lumen/Inner Diameter 1.32 mm In distribution
66-IT(AR30)-00481 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(DB9)-00529 Outer Diameter 1.83 mm In distribution
66-IT(BP5)-00510 Outer Diameter 1.83 mm In distribution
66-IT(BP21)-00585 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AR24)-00478 Outer Diameter 1.83 mm In distribution
66-IT-SG1P-00842 In distribution
66-IT(AR4)-00498 Outer Diameter 1.83 mm In distribution
66-IT(BP19)-00567 Outer Diameter 1.83 mm In distribution
66-IT(AR17)-00470 Outer Diameter 0.9 mm In distribution
66-IT(DB10)-00516 Lumen/Inner Diameter 1.6 mm In distribution
66-IT(AR23)-00874 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
Leksell Stereotactic System Neurosurgical Instruments Elekta Instrument AB 58
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
K121950 2012-07-26
K092192 2010-02-12
K092562 2009-09-18
K011775 2001-08-30
K011992 2001-08-14
K003776 2001-02-23

Recalls Naming This Product

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

Recalls naming the identifiers of microTargeting™ Insertion Tube with Stylet
Recalled by Identified by Initiated FDA class Root cause Reason Quantity Closed
FHC, Inc. 510(k) number 2024-10-04 Class I Process change control A complaint was received (MDR 3002250546-2024-00003) prompting an investigation. The investigation revealed a schematic for a spacer tube which is too long relative to the size of other components was included in the build order for Lot 244 8 packs of 5ea (40 total)
FHC, Inc. 510(k) number 2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
FHC, Inc. 510(k) number 2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
FHC, Inc. 510(k) number 2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
FHC, Inc. 510(k) number 2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
FHC, Inc. 510(k) number 2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
FHC, Inc. 510(k) number 2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
FHC, Inc. 510(k) number 2005-03-14 Not classified Other Potential for non-sterile pin to contaminate sterile field 169 units 2008-07-08

Recalls

9 of these are 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
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2018-05-10 Class II Device Design The FHC Depth Stop Adapter may cause damage to the lead and stylet when the depth stop screw is over-tightened onto the lead. This damage can manifest as low impedances or a short circuit between one or multiple electrode pairs in the lead, 2952 total 2019-04-30
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter may be overtightened and damage the implantable lead. 18 units 2015-02-25
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter
may be overtightened and damage the implantable lead.
37 2015-02-25
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter
may be overtightened and damage the implantable lead.
7 2015-02-25
2010-03-30 Not classified Device Design Fixation thumbscrew on the DBS depth stop adapter
may be overtightened and damage the implantable lead.
1 2015-02-25
2008-10-08 Not classified Process control Measuring fixture is incorrectly graduated. 5 units 2012-05-02
2005-10-31 Not classified Other Power Assist microTargeting System may advance beyond intended target 70 units 2006-06-07
2005-10-31 Not classified Other Power Assist microTargeting System may advance beyond intended target 230 units 2006-06-07

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