FDA UDI In Commercial Distribution 🇺🇸 United States

WishFIX

DI: B562PKEFC0416SS080 · Model: PK-EFC0416SS-08 · Wishbone Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
WishFIX
Primary DI
B562PKEFC0416SS080
Version / Model
PK-EFC0416SS-08
Catalog Number
PK-EFC0416SS
Company Name
Wishbone Medical, Inc.
Labeler DUNS
062355158
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2021-12-20
Public Version
3
Public Version Date
2023-09-18
Public Version Status
Update
Public Device Record Key
a7fbd2b4-0bd9-4bae-8b3e-43b7747008ff

Device Description

Procedure Kit, Curved 4-Hole X 16mm WishFIX Plate, Instruments and Solid Screws, SS

Device Characteristics

Single Use
Yes
Prescription Use (Rx)
Yes
Over the Counter (OTC)
No
Kit
Yes
Combination Product
No
HCT/P
No
Contains NRL
No
Not Made with NRL
Yes
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
Yes
Has Expiration Date
Yes
Has Donation ID
No

Sterilization

Is Sterile
Yes
Sterilization Prior Use
No

Product Codes

Code Name
OBT Plate, Bone, Growth Control, Pediatric, Epiphysiodesis

GMDN Terms

Code Name
46647 Orthopaedic fixation plate, non-bioabsorbable

Identifiers

Type ID
Primary B562PKEFC0416SS080

Premarket Submissions

Submission Number Supplement Number
K182704 000