FDA UDI In Commercial Distribution 🇺🇸 United States

AccelFix Spinal Fixation System

DI: 08800061316971 · Model: 2302-75145 · L&K BIOMED CO. ,LTD.
Product Codes
3
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

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Basic Information

Brand Name
AccelFix Spinal Fixation System
Primary DI
08800061316971
Version / Model
2302-75145
Catalog Number
2302-75145
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
2020-03-18
Public Version
3
Public Version Date
2024-09-11
Public Version Status
Update
Public Device Record Key
443a4006-6289-4f1b-8af4-b4a6e9603863

Device Description

Percutaneous Poly Screw Open Type Ø7.5 , 145mm

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

GMDN Terms

Code Name
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary 08800061316971

Premarket Submissions

Submission Number Supplement Number
K182544 000