FDA UDI In Commercial Distribution 🇺🇸 United States

AccelFix Spinal Fixation System

DI: 08800061327793 · Model: 8104-6555S · 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
08800061327793
Version / Model
8104-6555S
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
2019-08-17
Public Version
1
Public Version Date
2019-08-26
Public Version Status
New
Public Device Record Key
29a1906c-c973-4241-be74-eb66d1149cd0

Device Description

Reduction Poly Axial Screw Ø6.5 , 55mm

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
KWQ Appliance, Fixation, Spinal Intervertebral Body
KWP Appliance, Fixation, Spinal Interlaminal
NKB Thoracolumbosacral Pedicle Screw System

GMDN Terms

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

Identifiers

Type ID
Primary 08800061327793

Premarket Submissions

Submission Number Supplement Number
K182544 000