FDA UDI In Commercial Distribution 🇺🇸 United States

LnK Spinal Fixation System

DI: 08806189850519 · Model: 1067-60290 · L&K BIOMED CO. ,LTD.
Product Codes
5
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
LnK Spinal Fixation System
Primary DI
08806189850519
Version / Model
1067-60290
Catalog Number
1067-60290
Company Name
L&K BIOMED CO. ,LTD.
Labeler DUNS
631159324
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-08-31
Public Version
2
Public Version Date
2018-03-29
Public Version Status
Update
Public Device Record Key
0670435d-801c-4c73-a3e8-707ab7daca32

Device Description

L&K Biomed Rod, Straight, Double Stopper, TiTanium 6.0x290mm 1EA

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
No
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
KWP Appliance, Fixation, Spinal Interlaminal
KWQ Appliance, Fixation, Spinal Intervertebral Body
MNH Orthosis, Spondylolisthesis Spinal Fixation
MNI Orthosis, Spinal Pedicle Fixation
NKB Orthosis, Spinal Pedicle Fixation, For Degenerative Disc Disease

GMDN Terms

Code Name
61325 Bone-screw internal spinal fixation system, non-sterile

Identifiers

Type ID
Primary 08806189850519