FDA UDI In Commercial Distribution 🇺🇸 United States

SKYHAWK

DI: 18257200097036 · Model: 27-1571 · Orthofix US LLC
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
SKYHAWK
Primary DI
18257200097036
Version / Model
27-1571
Company Name
Orthofix US LLC
Labeler DUNS
927083808
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2019-03-12
Public Version
3
Public Version Date
2023-02-16
Public Version Status
Update
Public Device Record Key
d8f5b71a-d090-4595-8fc1-c9dae4fcd693

Device Description

16W X 55L X 12 DEG X 11H INTERBODY

Device Characteristics

Single Use
No
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
No
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
MAX Intervertebral fusion device with bone graft, lumbar

GMDN Terms

Code Name
38161 Metallic spinal interbody fusion cage

Identifiers

Type ID
Primary 18257200097036

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K162446 000