FDA UDI In Commercial Distribution 🇺🇸 United States

Ti-Fix OLIF Spacer

DI: M695P30101200 · Model: P-301012-0 · Tyber Medical LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Ti-Fix OLIF Spacer
Primary DI
M695P30101200
Version / Model
P-301012-0
Catalog Number
P-301012-0
Company Name
Tyber Medical LLC
Labeler DUNS
010968002
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-11-22
Public Version
2
Public Version Date
2020-02-24
Public Version Status
Update
Public Device Record Key
b6a7f522-d746-4bfa-b60a-e1c80330baa8

Device Description

Ti-Fix OLIF Spacer 30 x 10 x 12 (mm) x 0 °

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
No
PM Exempt
No
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
No
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
MAX Intervertebral fusion device with bone graft, lumbar
ODP Intervertebral fusion device with bone graft, cervical

GMDN Terms

Code Name
61230 Metal-polymer composite spinal interbody fusion cage

Identifiers

Type ID
Primary M695P30101200

Customer Contacts