FDA UDI Not in Commercial Distribution 🇺🇸 United States

Endoskeleton TAS

DI: M68223070313S0 · Model: 2307-0313-S · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Endoskeleton TAS
Primary DI
M68223070313S0
Version / Model
2307-0313-S
Catalog Number
2307-0313-S
Company Name
TITAN SPINE, LLC
Labeler DUNS
623316978
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-09-17
Public Version
7
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
08407746-c9ec-4eec-b36f-b35e6790d5bd
Distribution End Date
2020-09-21

Device Description

Interbody Fusion Device 7 Degree X-Large 13mm

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
Yes
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
OVD Intervertebral fusion device with integrated fixation, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary M68223070313S0

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K111626 000
K142589 000

Device Sizes

Type Value Unit Text
Device Size Text, specify Lordotic Angle 7 Deg
Height 13 Millimeter
Device Size Text, specify width(MLxAP), 40 x 27, mm
Width 40 Millimeter
Angle 7 degree
Depth 27 Millimeter