FDA UDI In Commercial Distribution 🇺🇸 United States

Savant Lumbar Interbody Fusion System

DI: B648C3053510 · Model: C305-351 · CURITEVA, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Savant Lumbar Interbody Fusion System
Primary DI
B648C3053510
Version / Model
C305-351
Company Name
CURITEVA, INC.
Labeler DUNS
074575332
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-04
Public Version
1
Public Version Date
2024-01-12
Public Version Status
New
Public Device Record Key
1206a99d-2bb4-46f4-ad3d-3ebccb70da77

Device Description

8mm (H) x 10mm (W) PLIF Lordotic Trial

Device Characteristics

Single Use
No
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
MAX Intervertebral Fusion Device With Bone Graft, Lumbar

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary B648C3053510

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K181589 000

Device Sizes

Type Value Unit Text
Height 8 Millimeter
Width 10 Millimeter