FDA UDI In Commercial Distribution 🇺🇸 United States

Smart Correction

DI: B562PK6020280 · Model: PK-602028 · Wishbone Medical, Inc.
Product Codes
1
GMDN Terms
1
Identifiers
1
Pkg Device Count
1

Basic Information

Brand Name
Smart Correction
Primary DI
B562PK6020280
Version / Model
PK-602028
Company Name
Wishbone Medical, Inc.
Labeler DUNS
062355158
Distribution Status
In Commercial Distribution
Device Count in Pkg
1
Record Status
Published
Publish Date
2023-03-24
Public Version
1
Public Version Date
2023-04-03
Public Version Status
New
Public Device Record Key
81298516-f64a-4ba9-beb6-cc1328d0c7f6

Device Description

Single Use 6mm Drill Sleeve Guide and Long Inserts - Sterile

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
LXH Orthopedic Manual Surgical Instrument

GMDN Terms

Code Name
48011 External orthopaedic fixation system, single-use

Identifiers

Type ID
Primary B562PK6020280

Customer Contacts