FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON® TAS

DI: 00191375050407 · Model: 2301-0003 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON® TAS
Primary DI
00191375050407
Version / Model
2301-0003
Catalog Number
2301-0003
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-09-30
Public Version
4
Public Version Date
2022-10-21
Public Version Status
Update
Public Device Record Key
870d5ce2-2455-425c-8dff-a8d7fc98e8ca
Distribution End Date
2021-02-24

Device Description

Awl Guide, ALIF

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
15275 Bone awl, reusable

Identifiers

Type ID
Primary 00191375050407

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111626 000

Device Sizes

Type Value Unit Text
Length 10 Inch