FDA UDI In Commercial Distribution 🇺🇸 United States

AccelFix Lumbar Plate System

DI: 08800061399929 · Model: 7102-6035S · L&K BIOMED CO. ,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AccelFix Lumbar Plate System
Primary DI
08800061399929
Version / Model
7102-6035S
Catalog Number
7102-6035S
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
2023-11-29
Public Version
1
Public Version Date
2023-12-07
Public Version Status
New
Public Device Record Key
dac28a57-6ec1-4d52-a85a-daf4a0a8ed19

Device Description

AccelFix Lumbar Plate Screw, (Fixed type, Dual thread), pi6.0, 35mm

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
Yes
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

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 08800061399929

Premarket Submissions

Submission Number Supplement Number
K192481 000