FDA UDI In Commercial Distribution 🇺🇸 United States

Kyocera Medical Technologies, Inc.

DI: 00841523159239 · Model: Skyway ACP · KYOCERA MEDICAL TECHNOLOGIES, INC.
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kyocera Medical Technologies, Inc.
Primary DI
00841523159239
Version / Model
Skyway ACP
Catalog Number
1061-240-018
Company Name
KYOCERA MEDICAL TECHNOLOGIES, INC.
Labeler DUNS
116995646
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2024-01-09
Public Version
1
Public Version Date
2024-01-17
Public Version Status
New
Public Device Record Key
c8c0d075-a784-4780-9a7f-0d4591a545bc

Device Description

4.0mm x 18mm Fixed Angle, Self Drilling

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
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OVE Intervertebral Fusion Device With Integrated Fixation, Cervical
KWQ Appliance, Fixation, Spinal Intervertebral Body

GMDN Terms

Code Name
46653 Spinal fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary 00841523159239

Premarket Submissions

Submission Number Supplement Number
K231766 000