FDA UDI In Commercial Distribution 🇺🇸 United States

AFX

DI: 00817906028348 · Model: P07 N1011 · IN2BONES USA, LLC
Product Codes
2
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
AFX
Primary DI
00817906028348
Version / Model
P07 N1011
Company Name
IN2BONES USA, LLC
Labeler DUNS
079700711
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-10-22
Public Version
3
Public Version Date
2021-04-21
Public Version Status
Update
Public Device Record Key
98cf6c23-f3c3-4bbb-98ed-a2f6e3c824fa

Device Description

LATERAL FIBULA PLATE, 3-HOLE, LEFT, TRIAL

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
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
No
Has Donation ID
No

Sterilization

Is Sterile
No
Sterilization Prior Use
Yes
Sterilization Methods
Moist Heat or Steam Sterilization

Product Codes

Code Name
HWC Screw, Fixation, Bone
HRS Plate, Fixation, Bone

GMDN Terms

Code Name
47807 Surgical implant/trial-implant/sizer holder, reusable

Identifiers

Type ID
Primary 00817906028348

Premarket Submissions

Submission Number Supplement Number
K181113 000