FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON TAS

DI: M682231294080 · Model: 2312-9408 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON TAS
Primary DI
M682231294080
Version / Model
2312-9408
Catalog Number
2312-9408
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
7
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
d13a1f9f-9e53-47fa-b05c-d88153870251
Distribution End Date
2020-09-21

Device Description

12 Deg Lordotic, Trial, Hybrid, 8mm

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
No
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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
44788 Spinal implant trial

Identifiers

Type ID
Primary M682231294080

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111626 000

Device Sizes

Type Value Unit Text
Height 8 Millimeter
Width 36 Millimeter
Depth 21 Millimeter