Microtargeting™ Procedure Kit
microTargeting Platform Procedure Consumables Kit, 1x, sterile, for use with mT or STar Drive, mT Platform and Guideline 4000 LP+. Contains: 44975L: D.ZAP Tungsten Differential Electrode -…
microTargeting Platform Procedure Consumables Kit, 1x, sterile, for use with mT or STar Drive, mT Platform and Guideline 4000 LP+. Contains: 44975L: D.ZAP Tungsten Differential Electrode – – 220.72mm electrode length, 10mm differential, 205.72mm protective tube length, DZAP(L) 1Meg, 0.55mm od. 66-DA-SD: Sterile Drape Sleeve for motor 66-EL-LP: Patient Lead for Guideline 4000 LP+ 66-IT-03P: Sterile Single Insertion Tube Set – IT(MP1) – 184.1mm tube length, 1.83mm od, 1.6mm id with Stylet PT(MP1) – Diameter reduction tube 0.58mm id
5manufacturers in China registered for this device type
1catalogue number
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.
| 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
| 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 | 2021-12-22 (version 7) |
Specifications
| MRI safety | MR Unsafe |
|---|---|
| Sterilisation | Ethylene Oxide, Moist Heat or Steam Sterilization |
| 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 humidity 0 to 95 % RH; Storage environment temperature 0 to 40 °C |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| KT-PPK-S-00366 | In distribution |
Same 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 Stereotactic System Neurosurgical Instruments | Elekta Instrument AB | 58 |
| Leksell Vantage Stereotactic System | Elekta Instrument AB | 53 |
| Stealth Autoguide™ System | Medtronic Navigation, Inc. | 50 |
Showing 12 of 1,137. All products under Neurological Stereotaxic Instrument
510(K) Clearances
| 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
14 recalls name this product by its own identifiers, the 510(k) it is cleared under.
| 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 | 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 | 2009-12-28 | Not classified | Software change control | The raster tab for the GL4K version 1.4 software may assign incorrect depths for waveform recordings and if used to identify the implantation target for the DBS lead, the implant may be placed in the wrong location. | 10 | 2010-03-18 |
| FHC, Inc. | 510(k) number | 2008-10-08 | Not classified | Process control | Measuring fixture is incorrectly graduated. | 5 units | 2012-05-02 |
| FHC, Inc. | 510(k) number | 2005-10-31 | Not classified | Other | Power Assist microTargeting System may advance beyond intended target | 70 units | 2006-06-07 |
| FHC, Inc. | 510(k) number | 2005-10-31 | Not classified | Other | Power Assist microTargeting System may advance beyond intended target | 230 units | 2006-06-07 |
| 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
7 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.
| 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 |
| 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 |
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.