FDA UDI In Commercial Distribution 🇺🇸 United States

WishBone K-Wire System

DI: B56251904100709G10 · Model: 51-904-100709G-1 · Wishbone Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WishBone K-Wire System
Primary DI
B56251904100709G10
Version / Model
51-904-100709G-1
Catalog Number
51-904-100709G-1
Company Name
Wishbone Medical, Inc.
Labeler DUNS
062355158
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2022-07-18
Public Version
3
Public Version Date
2023-05-03
Public Version Status
Update
Public Device Record Key
34bf8a78-d193-4094-9cae-f5572e3fe4df

Device Description

Double K-wire Soft Tissue Protector, 0.70mm/0.90mm

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
Yes
Has Serial Number
No
Has Lot/Batch Number
Yes
Has Manufacturing Date
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
58927 Orthopaedic prosthesis implantation positioning instrument, single-use

Identifiers

Type ID
Primary B56251904100709G10