FDA UDI Not in Commercial Distribution 🇺🇸 United States

ENDOSKELETON TL

DI: M682720010240 · Model: 7200-1024 · TITAN SPINE, LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
ENDOSKELETON TL
Primary DI
M682720010240
Version / Model
7200-1024
Catalog Number
7200-1024
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
5
Public Version Date
2020-12-09
Public Version Status
Update
Public Device Record Key
9162d50f-b0ca-4e00-a28c-60d47da4762a
Distribution End Date
2020-09-21

Device Description

MEDIUM, UP, CUP CURETTE

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
31335 Bone curette, reusable

Identifiers

Type ID
Primary M682720010240

Customer Contacts

Device Sizes

Type Value Unit Text
Length 16 Inch