FDA UDI In Commercial Distribution 🇺🇸 United States

PHOENIX ANKLE NAIL SYSTEM

DI: 00887868097652 · Model: 14-444180 · Biomet Orthopedics, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Let the assistant research this device

The Research Assistant compiles product codes, classification, clearances and adverse events for this device — and cites every record.

Free to try · every answer cites its records

Basic Information

Brand Name
PHOENIX ANKLE NAIL SYSTEM
Primary DI
00887868097652
Version / Model
14-444180
Catalog Number
14-444180
Company Name
Biomet Orthopedics, LLC
Labeler DUNS
129278169
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2015-10-24
Public Version
7
Public Version Date
2026-02-09
Public Version Status
Update
Public Device Record Key
9f6fb49a-6e2b-4c49-a705-6f6d59df97c4

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
HSB ROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES
KTT APPLIANCE, FIXATION, NAIL/BLADE/PLATE COMBINATION, MULTIPLE COMPONENT

GMDN Terms

Code Name
46139 Bone nail implantable cap

Identifiers

Type ID
Primary 00887868097652

Customer Contacts

Premarket Submissions

Submission Number Supplement Number
K071395 000
K072161 000

Device Sizes

Type Value Unit Text
Device Size Text, specify 12MM Ø 0 MM