Achievecas
Achievecas Reflection Passive Spheres 4 Quantity 1 Pack Sterile
5manufacturers in China registered for this device type
43catalogue numbers in this listing
8510(k) clearances naming this product 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 | Smith & Nephew, Inc., United States |
|---|---|
| FDA product code | HAW |
| Device type | Neurological Stereotaxic Instrument |
| Device class | Class 2 |
| Regulation | 21 CFR 882.4560 |
| Establishment | Contract manufacturer, Remanufacturer, Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K033341 |
| Record published | 2015-08-29 |
| Record revised | 2023-10-04 (version 9) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Supplied sterile | Yes |
| Single use | Yes |
| Prescription | Prescription only |
| Label carries | lot or batch number, expiry date |
| Distribution end date | 2023-10-04 |
Catalogue Numbers
| Catalogue number | Size | Per pack | Status |
|---|---|---|---|
| 74452322 | In distribution | ||
| 74451117 | In distribution | ||
| 74452313 | In distribution | ||
| 74471206 | In distribution | ||
| 74473200 | In distribution | ||
| 74451007 | In distribution | ||
| 74452314 | In distribution | ||
| 74471201 | Withdrawn | ||
| 74451009 | Withdrawn | ||
| 74452005 | Withdrawn | ||
| 74452332 | Withdrawn | ||
| 74452317 | Withdrawn | ||
| 74453002 | Withdrawn | ||
| 74452310 | Withdrawn | ||
| 74452318 | Withdrawn | ||
| 74451224 | Withdrawn | ||
| 74452003 | Withdrawn | ||
| 74452334 | Withdrawn | ||
| 74453001 | Withdrawn | ||
| 74451223 | Withdrawn | ||
| 74452001 | Withdrawn | ||
| 74471203 | Withdrawn | ||
| 74452308 | Withdrawn | ||
| 74451119 | Withdrawn | ||
| 74451008 | Withdrawn | ||
| 74451006 | Withdrawn | ||
| 74471202 | Withdrawn | ||
| 74471205 | Withdrawn | ||
| 74452330 | Withdrawn | ||
| 71470901 | Withdrawn | ||
| 74452338 | Withdrawn | ||
| 74452331 | Withdrawn | ||
| 74451221 | Withdrawn | ||
| 74452301 | Withdrawn | ||
| 74451226 | Withdrawn | ||
| 74452339 | Withdrawn | ||
| 74451511 | Withdrawn | ||
| 74453003 | Withdrawn | ||
| 74452319 | Withdrawn | ||
| 74452341 | Withdrawn | ||
| 74482004 | 4 | Withdrawn | |
| 74451018 | Withdrawn | ||
| 74452307 | Withdrawn |
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 |
|---|---|
| K083565 | 2009-02-20 |
| K082267 | 2008-10-29 |
| K080875 | 2008-07-18 |
| K033341 | 2004-09-10 |
| K021798 | 2002-12-09 |
| K021815 | 2002-10-17 |
| K022460 | 2002-08-19 |
| K012938 | 2002-02-08 |
Recalls Naming This Product
1 recall names this product by its own identifier, the 510(k) it is cleared under.
| Recalled by | Identified by | Initiated | FDA class | Root cause | Reason | Quantity | Closed |
|---|---|---|---|---|---|---|---|
| Zimmer, Inc. | 510(k) number | 2006-04-27 | Not classified | Device Design | The three-point array may break during use, resulting in surgical delay and an increased risk of infection. | 239 | 2009-03-11 |
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.