FDA UDI Not in Commercial Distribution 🇺🇸 United States

K2™ Hemi Toe Implant System

DI: 10381780279440 · Model: 203200 · Ascension Orthopedics, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
2
Pkg Device Count
1

Basic Information

Brand Name
K2™ Hemi Toe Implant System
Primary DI
10381780279440
Version / Model
203200
Catalog Number
203200
Company Name
Ascension Orthopedics, Inc.
Labeler DUNS
942377524
Distribution Status
Not in Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2018-04-10
Public Version
6
Public Version Date
2023-10-04
Public Version Status
Update
Public Device Record Key
1e0895b8-fa8c-4659-8324-5835c6e48e8f
Distribution End Date
2023-03-31

Device Description

K2 HEMI REAMER

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
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
HTO REAMER

GMDN Terms

Code Name
45114 Bone-resection orthopaedic reamer, reusable

Identifiers

Type ID
Secondary M2482032001
Primary 10381780279440

Customer Contacts

Device Sizes

Type Value Unit Text
Device Size Text, specify 59.8mm Length x 9.40mm Diameter