FDA UDI In Commercial Distribution 🇺🇸 United States

KASILOF Cervical Plate System

DI: B644KCP14780 · Model: KCP1-478 · KAHTNU SURGICAL
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
KASILOF Cervical Plate System
Primary DI
B644KCP14780
Version / Model
KCP1-478
Company Name
KAHTNU SURGICAL
Labeler DUNS
081208474
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-03-05
Public Version
1
Public Version Date
2021-03-15
Public Version Status
New
Public Device Record Key
ecb7c98c-cb78-4791-9d44-468a90b0f253

Device Description

KASILOF CERVICAL PLATE, 4 LEVEL, 78mm

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
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
No
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
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

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

Identifiers

Type ID
Primary B644KCP14780

Premarket Submissions

Submission Number Supplement Number
K203154 000