GPS
GPS Femoral Adjustable Resection Guide
5manufacturers in China registered for this device type
16catalogue numbers in this listing
2recalls on this code
Who Else Makes It
Concentrated in Jiangsu (2), Shanghai (1), Guangdong (1). 3 of them are registered as contract manufacturers, able to build to a buyer’s own specification.
| Manufacturer | City | Province | Registered as | Device types |
|---|---|---|---|---|
| Apex (Guangzhou) Tools & Orthopedics Company | Guangzhou | Guangdong | Contract manufacturer | 62 |
| 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 |
Record
| Listed by | Exactech, Inc., United States |
|---|---|
| FDA product code | OLO |
| Device type | Orthopedic Stereotaxic Instrument |
| Device class | Class 2 |
| Regulation | 21 CFR 882.4560 |
| Establishment | Specification developer, Repacker / relabeller, Complaint-file establishment, Manufacturer, Exporter |
| 510(k) | K162567 |
| Record published | 2022-08-25 |
| Record revised | 2025-08-27 (version 2) |
Specifications
| MRI safety | Labeling does not contain MRI Safety Information |
|---|---|
| Sterilisation | Moist Heat or Steam Sterilization |
| Prescription | Prescription only |
| Label carries | lot or batch number |
| Sizes | Angle 16 °; outer diameter 3.2 mm |
| Distribution end date | 2024-06-13 |
Catalogue Numbers
| Catalogue number | Size | Status |
|---|---|---|
| 531-29-15 | Angle 16 ° | In distribution |
| 531-27-05 | RIGHT | In distribution |
| 531-29-14 | LEFT | In distribution |
| SPI-046603 | In distribution | |
| 531-15-07 | Outer Diameter 3.2 mm | In distribution |
| 531-01-04 | In distribution | |
| 02-521-10-0003 | In distribution | |
| 531-07-50 | In distribution | |
| 02-521-90-0001 | In distribution | |
| 531-27-63 | In distribution | |
| 02-521-10-0006 | Withdrawn | |
| 02-521-10-0004 | Withdrawn | |
| 02-521-20-2003 | Withdrawn | |
| 02-521-20-1003 | Withdrawn | |
| 02-521-20-1002 | Withdrawn | |
| 02-521-78-0000 | Withdrawn |
Same Product Code
| Product | Sold by | Catalogue numbers |
|---|---|---|
| Valence Robotic Navigation System | Alphatec Spine, Inc. | 813 |
| Olympic | Astura Medical | 684 |
| Excelsius GPS | Globus Medical, Inc. | 383 |
| Orthopedic Stereotaxic Instrument | Medtronic Navigation, Inc. | 356 |
| Masada | Astura Medical | 335 |
| Excelsiusgps | Globus Medical, Inc. | 297 |
| Invictus | Alphatec Spine, Inc. | 235 |
| OrthAlign Plus | OrthAlign, Inc. | 210 |
| Arvis ® | Kico Knee Innovation Company | 174 |
| OMNIBotics | Omni Life Science, Inc. | 150 |
| CD Horizon® Spinal System | Medtronic Sofamor Danek, Inc. | 137 |
| Navigation Instruments | VB Spine LLC | 135 |
Showing 12 of 1,127. All products under Orthopedic Stereotaxic Instrument
Recalls Naming This Product
4 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 |
|---|---|---|---|---|---|---|---|
| Exactech, Inc. | 510(k) number | 2023-06-05 | Class II | Process control | The ball and spring housed within the locking mechanism of the handle can dislodge during disassembly or during impaction. | 250 devices | |
| Blue Ortho | 510(k) number | 2020-09-10 | Class II | Other | Appropriateness of the language used in the Tracker reprocessing instruction. Reason is that some Low Temperature sterilization conditions mentioned in the IFUs are approved based on rational documents. | 3471 units | 2023-05-31 |
| Blue Ortho | 510(k) number | 2019-09-22 | Class II | Software design | The navigated values displayed when using the LPI instrumentation are incorrect due to software inconsistencies (wrong data loaded). | 7 units | 2020-07-23 |
| Exactech, Inc. | 510(k) number | 2017-07-11 | Class II | Nonconforming Material/Component | Vix Bit may fracture during use. | 41 devices | 2021-04-22 |
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.