FDA UDI In Commercial Distribution 🇺🇸 United States

Tranquil-L™

DI: B6785229330 · Model: 522933 · NEXUS SPINE, L.L.C.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Tranquil-L™
Primary DI
B6785229330
Version / Model
522933
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
e4fade50-2614-4a2c-9864-5df8af142281

Device Description

Steerable IBD 16x10x32, 6 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
Yes
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
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary B6785229330

Premarket Submissions

Submission Number Supplement Number
K170297 000
K181483 000
K181702 000

Device Sizes

Type Value Unit Text
Width 10 Millimeter
Length 32 Millimeter
Height 16 Millimeter