Pediatric Long Bone Combo K-Wire System

GUDID B562KITKWILBONE0

WISHBONE MEDICAL, INC.

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Primary Device IDB562KITKWILBONE0
NIH Device Record Key16c37fb4-8e67-4db6-a9af-b3415d3e4a74
Commercial Distribution StatusIn Commercial Distribution
Brand NamePediatric Long Bone Combo K-Wire System
Version Model NumberKIT-KWI-LBONE
Company DUNS062355158
Company NameWISHBONE MEDICAL, INC.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kittrue
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB562KITKWILBONE0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HTYPin, Fixation, Smooth

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2019-07-02
Device Publish Date2019-03-19

Devices Manufactured by WISHBONE MEDICAL, INC.

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