Feetfix™ Platform 302071
GUDID 00841439110003
Feetfix™ Platform
MEDTEC, INC.
Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner Radiological arm/leg positioner| Primary Device ID | 00841439110003 |
| NIH Device Record Key | 0c398a10-87dd-4adb-ad4b-603443b0ee29 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | Feetfix™ Platform |
| Version Model Number | 302071 |
| Catalog Number | 302071 |
| Company DUNS | 103977526 |
| Company Name | MEDTEC, INC. |
| Device Count | 1 |
| DM Exempt | true |
| Pre-market Exempt | false |
| MRI Safety Status | Labeling does not contain MRI Safety Information |
| Human Cell/Tissue Product | false |
| Device Kit | false |
| Device Combination Product | false |
| Single Use | false |
| Lot Batch | true |
| Serial Number | false |
| Manufacturing Date | true |
| Expiration Date | false |
| Donation Id Number | false |
| Contains Natural Rubber Latex | false |
| Labeled No Natural Rubber Latex | false |
| RX Perscription | true |
| OTC Over-The-Counter | false |
Customer Support Contacts
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00841439110003 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K060737
FDA Product Code
| IYE | Accelerator, linear, medical |
Sterilization
| Steralize Prior To Use | false |
| Device Is Sterile | false |
Device Entry Metadata
| Public Version Status | Update |
| Device Record Status | Published |
| Public Version Number | 5 |
| Public Version Date | 2019-05-31 |
| Device Publish Date | 2017-08-02 |
On-Brand Devices [Feetfix™ Platform]
| 00841439110003 | Feetfix™ Platform |
| 00841439101292 | Feetfix™ Platform |
Trademark Results [Feetfix]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 FEETFIX 98185639 not registered Live/Pending |
Fix Digital Incorporated 2023-09-18 |
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