ProLift Wedge
GUDID 00190837152840
Life Spine, Inc.
Metallic spinal interbody fusion cage| Primary Device ID | 00190837152840 |
| NIH Device Record Key | 7c4ee8ef-7f75-4704-873a-27006e09f3c9 |
| Commercial Distribution Status | In Commercial Distribution |
| Brand Name | ProLift Wedge |
| Version Model Number | L180-103 |
| Company DUNS | 183641617 |
| Company Name | Life Spine, Inc. |
| Device Count | 1 |
| DM Exempt | false |
| 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 | false |
| 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 |
Device Identifiers
| Device Issuing Agency | Device ID |
|---|---|
| GS1 | 00190837152840 [Primary] |
FDA Pre-market Approvals/Notifications & deNovo
- Premarket Notification: K203361
FDA Product Code
| MAX | Intervertebral Fusion Device With Bone Graft, Lumbar |
Sterilization
| Steralize Prior To Use | true |
| Device Is Sterile | false |
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
[00190837152840]
Moist Heat or Steam Sterilization
Device Entry Metadata
| Public Version Status | New |
| Device Record Status | Published |
| Public Version Number | 1 |
| Public Version Date | 2022-11-25 |
| Device Publish Date | 2022-11-17 |
On-Brand Devices [ProLift Wedge]
| 00190837107741 | 70-1028-0815 |
| 00190837107697 | 70-1028-1015 |
| 00190837107758 | 70-1028-0915 |
| 00190837152369 | 70-1228-1615 |
| 00190837152352 | 70-1228-1415 |
| 00190837152345 | 70-1228-1215 |
| 00190837152338 | 70-1228-1115 |
| 00190837152321 | 70-1228-1015 |
| 00190837152314 | 70-1228-0915 |
| 00190837152307 | 70-1228-0815 |
| 00190837107734 | 70-1028-1615 |
| 00190837107727 | 70-1028-1415 |
| 00190837107710 | 70-1028-1215 |
| 00190837107703 | 70-1028-1115 |
| 00190837143046 | 180-103 |
| 00190837140779 | 180-102 |
| 00190837145651 | 70-1028-1315 |
| 00190837152840 | L180-103 |
| 00190837145668 | 70-1028-1515 |
| 00190837154868 | 114-280-5 |
| 00190837152703 | L129-521 |
| 00190837152697 | L129-520 |
| 00190837152680 | L129-519 |
| 00190837152673 | L129-518 |
| 00190837152666 | L129-517 |
| 00190837152659 | L129-516 |
| 00190837152642 | L129-515 |
| 00190837152635 | L129-514 |
| 00190837152628 | L129-513 |
| 00190837152611 | L129-512 |
| 00190837152604 | L129-511 |
| 00190837152598 | L114-280-5 |
| 00190837152581 | L114-280-4 |
| 00190837152574 | L114-280-2 |
| 00190837152567 | L114-280-1 |
| 00190837145644 | 114-280-4 |
| 00190837145620 | 114-280-2 |
| 00190837145613 | 114-280-1 |
| 00190837200060 | L180-104 |
| 00190837156077 | 180-104 |
Trademark Results [ProLift Wedge]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 PROLIFT WEDGE 97501024 not registered Live/Pending |
Life Spine, Inc. 2022-07-13 |
© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.