FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON TO

DI: M682390010010 · Model: 3900-1001 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON TO
Primary DI
M682390010010
Version / Model
3900-1001
Catalog Number
3900-1001
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2016-09-17
Public Version
10
Public Version Date
2022-09-16
Public Version Status
Update
Public Device Record Key
6f170947-8d54-4aa1-95ba-badefc59b0fa
Distribution End Date
2020-09-21

Device Description

TRAY SYSTEM

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
Yes
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
12143 Instrument tray, reusable

Identifiers

Type ID
Primary M682390010010

Customer Contacts

Device Sizes

Type Value Unit Text
Width 10 Inch
Height 4 Inch
Length 21 Inch