FDA UDI In Commercial Distribution 🇺🇸 United States

Kestrel®

DI: M711UT55250 · Model: UT5525 · Innovasis, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Kestrel®
Primary DI
M711UT55250
Version / Model
UT5525
Catalog Number
UT5525
Company Name
Innovasis, Inc.
Labeler DUNS
156567492
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-09-30
Public Version
4
Public Version Date
2024-01-03
Public Version Status
Update
Public Device Record Key
7e6e4898-8227-4125-8fe0-d2e755c7e008

Device Description

Ti 6Al 4V (ELI)

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
Yes
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
46651 Spinal bone screw, non-bioabsorbable

Identifiers

Type ID
Primary M711UT55250

Customer Contacts

Phone
801-261-2236

Premarket Submissions

Submission Number Supplement Number
K181063 000

Device Sizes

Type Value Unit Text
Outer Diameter 5.5 Millimeter
Length 25 Millimeter