FDA UDI In Commercial Distribution 🇺🇸 United States

Stronghold® C 3D Titanium Interbody Device System

DI: 10840642161922 · Model: SW18105-0615 · Spine Wave, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Stronghold® C 3D Titanium Interbody Device System
Primary DI
10840642161922
Version / Model
SW18105-0615
Catalog Number
SW18105-0615
Company Name
Spine Wave, Inc.
Labeler DUNS
067789763
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-06
Public Version
1
Public Version Date
2021-12-14
Public Version Status
New
Public Device Record Key
7346e0ad-9755-4c35-8197-8a6656ad69db

Device Description

Cervical Titanium Cage - Anatomical 15 mm x 12 mm x 6 mm

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
ODP Intervertebral Fusion Device With Bone Graft, Cervical

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 10840642161922

Customer Contacts

Phone
203-944-9494

Premarket Submissions

Submission Number Supplement Number
K181229 000

Device Sizes

Type Value Unit Text
Width 15 Millimeter
Length 12 Millimeter
Height 6 Millimeter