FDA UDI In Commercial Distribution 🇺🇸 United States

Onyx Frontier™

DI: 00763000511272 · Model: ONYXNG25008UX · MEDTRONIC, INC.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Onyx Frontier™
Primary DI
00763000511272
Version / Model
ONYXNG25008UX
Company Name
MEDTRONIC, INC.
Labeler DUNS
006261481
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-06-11
Public Version
1
Public Version Date
2022-06-21
Public Version Status
New
Public Device Record Key
59eb3ecc-7152-4036-b929-10c708c785a7

Device Description

STENT ONYXNG25008UX ONYX 2.50X08RX

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
Yes
HCT/P
No
Contains NRL
No
Not Made with NRL
No
MRI Safety
MR Conditional
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
Yes
Sterilization Prior Use
No

Product Codes

Code Name
NIQ Coronary drug-eluting stent

GMDN Terms

Code Name
56284 Drug-eluting coronary artery stent, non-bioabsorbable-polymer-coated

Identifiers

Type ID
Primary 00763000511272

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
P160043 055

Device Sizes

Type Value Unit Text
Stent Length 8.0 Millimeter
Stent Diameter 2.5 Millimeter

Storage Conditions

Type
Storage Environment Temperature
Temperature Range
15 – 30 Degrees Celsius