FDA UDI In Commercial Distribution 🇺🇸 United States

OneLIF™

DI: G07001131920100 · Model: 011-319-2010 · Novapproach Spine LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
OneLIF™
Primary DI
G07001131920100
Version / Model
011-319-2010
Catalog Number
011-319-2010
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
38c277ec-e2f4-435d-bf40-5944258ba8d0

Device Description

Trial-OneLIF Interbody, Large, 19 Degree, 20mm X 10mm

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
No
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
44788 Spinal implant trial

Identifiers

Type ID
Primary G07001131920100

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K211769 000