FDA UDI In Commercial Distribution 🇺🇸 United States

Adaptix™ PEEK Interbody System with Nanotechnology

DI: 00814216028389 · Model: 74332809 · NANOVIS SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Adaptix™ PEEK Interbody System with Nanotechnology
Primary DI
00814216028389
Version / Model
74332809
Catalog Number
74332809
Company Name
NANOVIS SPINE, LLC
Labeler DUNS
079898044
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-10-30
Public Version
2
Public Version Date
2025-07-21
Public Version Status
Update
Public Device Record Key
9c0ff099-831e-4299-9bbc-406f826ee0d2

Device Description

Adaptix PEEK w/ Nano 28 x 9 x 10

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
61230 Metal-polymer composite spinal interbody fusion cage

Identifiers

Type ID
Primary 00814216028389

Customer Contacts

Phone
8779076266

Premarket Submissions

Submission Number Supplement Number
K241605 000

Device Sizes

Type Value Unit Text
Length 28 Millimeter
Width 10 Millimeter
Height 9 Millimeter