FDA UDI In Commercial Distribution 🇺🇸 United States

Inspire Lumbar Interbody Fusion System

DI: B648C43428091381 · Model: C434-280913-8 · CURITEVA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Inspire Lumbar Interbody Fusion System
Primary DI
B648C43428091381
Version / Model
C434-280913-8
Company Name
CURITEVA, INC.
Labeler DUNS
074575332
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-06-26
Public Version
1
Public Version Date
2024-07-04
Public Version Status
New
Public Device Record Key
9d3bb876-f97c-499a-8a46-060571f33a0f

Device Description

Porous PEEK TLIF Spacer, 28 x 9 x 13mm, 8 deg

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
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
Yes
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
60762 Polymeric spinal interbody fusion cage

Identifiers

Type ID
Primary B648C43428091381

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K233744 000

Device Sizes

Type Value Unit Text
Width 9 Millimeter
Height 13 Millimeter
Length 28 Millimeter
Angle 8 degree