FDA UDI In Commercial Distribution 🇺🇸 United States

AccelFix Spinal Fixation System

DI: 08800061311815 · Model: 2405-5530 · L&K BIOMED CO. ,LTD.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AccelFix Spinal Fixation System
Primary DI
08800061311815
Version / Model
2405-5530
Catalog Number
2405-5530
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
2019-12-12
Public Version
1
Public Version Date
2019-12-20
Public Version Status
New
Public Device Record Key
c2352be2-b0c8-4ba7-95fe-0a4eea7213f5

Device Description

Percutaneous Poly Screw Closed Type Ø5.5 , 30mm

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
NKB Thoracolumbosacral Pedicle Screw System
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

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

Identifiers

Type ID
Primary 08800061311815

Premarket Submissions

Submission Number Supplement Number
K182544 000