FDA UDI In Commercial Distribution 🇺🇸 United States

PathLoc-C Posterior Cervical Fixation System

DI: 08806344308053 · Model: 6316-4022 · L&K BIOMED CO. ,LTD.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
PathLoc-C Posterior Cervical Fixation System
Primary DI
08806344308053
Version / Model
6316-4022
Catalog Number
6316-4022
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
2016-07-27
Public Version
3
Public Version Date
2018-07-06
Public Version Status
Update
Public Device Record Key
ea29e9bc-1403-472b-b8f2-25a1701e225b

Device Description

PathLoc-C Cervical MIS Screw(Open Type, Sleeve 60mm) 4.0x22mm 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
NKG Orthosis, Cervical Pedicle Screw Spinal Fixation

GMDN Terms

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

Identifiers

Type ID
Primary 08806344308053

Premarket Submissions

Submission Number Supplement Number
K153439 000