FDA UDI Not in Commercial Distribution 🇺🇸 United States

Endoskeleton TCS

DI: M682530238200 · Model: 5302-3820 · TITAN SPINE, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Endoskeleton TCS
Primary DI
M682530238200
Version / Model
5302-3820
Catalog Number
5302-3820
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
8
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
bfc05e46-8af7-4683-95b7-011440d8b1db
Distribution End Date
2020-09-21

Device Description

Interbody Fusion Device 3.8mm Implant Locking Bone Screw 20mm

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
ODP Intervertebral fusion device with bone graft, cervical
OVE Intervertebral fusion device with integrated fixation, cervical

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M682530238200

Customer Contacts

Device Sizes

Type Value Unit Text
Length 20 Millimeter
Outer Diameter 3.8 Millimeter
Device Size Text, specify Locking Bone Screw
Device Size Text, specify 3.8mm Diameter, 20mm Length, No. 8 Hexalobe