Superior Mid-Shaft Narrow Straight Clavicle Plate Procedure Kit 8 hole Right

GUDID B562PKSMC0835NSRTI0

WISHBONE MEDICAL, INC.

Orthopaedic fixation plate kit, non-bioabsorbable, sterile Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial Orthopaedic fixation plate kit, non-bioabsorbable, non-antimicrobial
Primary Device IDB562PKSMC0835NSRTI0
NIH Device Record Key40c71d2c-d9c0-404e-877a-7347600e541d
Commercial Distribution StatusIn Commercial Distribution
Brand NameSuperior Mid-Shaft Narrow Straight Clavicle Plate Procedure Kit 8 hole Right
Version Model NumberPK-SMC0835NSR-TI
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 Latextrue
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCB562PKSMC0835NSRTI0 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPlate, Fixation, Bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2019-09-16
Device Publish Date2019-09-06

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