FDA UDI In Commercial Distribution 🇺🇸 United States

TIGER Spine System

DI: M72560345500 · Model: 60345-50 · CORELINK LLC
Product Codes
4
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
TIGER Spine System
Primary DI
M72560345500
Version / Model
60345-50
Company Name
CORELINK LLC
Labeler DUNS
064191453
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2014-09-19
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
2cef82c2-7b44-4b2e-ba59-f5259eba2625

Device Description

POSTED SCREW PLATE 4 SLOT 20MM, 33.5MM, 33.5MM, 20MM

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
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
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease
KWP Appliance, Fixation, Spinal Interlaminal
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation

GMDN Terms

Code Name
43257 Bone-screw internal spinal fixation system

Identifiers

Type ID
Primary M72560345500

Customer Contacts

Phone
314-863-5401

Device Sizes

Type Value Unit Text
Device Size Text, specify Slot 3 33.5 mm
Device Size Text, specify Slot 20 mm
Device Size Text, specify Slot 33.5 mm
Device Size Text, specify Slot2 20 mm