FDA UDI In Commercial Distribution 🇺🇸 United States

Tranquil-C™

DI: B6785224140 · Model: 522414 · NEXUS SPINE, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tranquil-C™
Primary DI
B6785224140
Version / Model
522414
Company Name
NEXUS SPINE, L.L.C.
Labeler DUNS
028137605
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-17
Public Version
1
Public Version Date
2021-12-27
Public Version Status
New
Public Device Record Key
48b714f0-3261-482f-89f8-056e317e4862

Device Description

Cervical IBD 6x16x13, Planar, 12 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
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary B6785224140

Premarket Submissions

Submission Number Supplement Number
K170297 000
K181483 000

Device Sizes

Type Value Unit Text
Width 16 Millimeter
Length 13 Millimeter
Height 6 Millimeter