FDA UDI In Commercial Distribution 🇺🇸 United States

TPLIF Interbody System

DI: M695002P2811080 · Model: 002-P281108 · Tyber Medical LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TPLIF Interbody System
Primary DI
M695002P2811080
Version / Model
002-P281108
Catalog Number
002-P281108
Company Name
Tyber Medical LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-12-19
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
9f5796cf-7b76-4011-b16c-d090f2413e4f

Device Description

PLIF 28 x 11 x 0 deg Trial

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
No
PM Exempt
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
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
LXH ORTHOPEDIC MANUAL SURGICAL INSTRUMENT

GMDN Terms

Code Name
61230 Metal-polymer composite spinal interbody fusion cage

Identifiers

Type ID
Primary M695002P2811080

Customer Contacts