FDA UDI In Commercial Distribution 🇺🇸 United States

OneLIF™

DI: G07001501200010 · Model: 015-012-0001 · Novapproach Spine LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OneLIF™
Primary DI
G07001501200010
Version / Model
015-012-0001
Catalog Number
015-012-0001
Company Name
Novapproach Spine LLC
Labeler DUNS
059260001
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-02-03
Public Version
1
Public Version Date
2022-02-11
Public Version Status
New
Public Device Record Key
8219f505-8a79-4cc5-8a03-07bd200a4b16

Device Description

Tamp Attachment

Device Characteristics

Single Use
No
Prescription Use (Rx)
No
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
Labeling does not contain MRI Safety Information
Direct Marking Exempt
Yes
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
64192 Internal spinal fixation procedure kit, reusable

Identifiers

Type ID
Primary G07001501200010

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K211769 000