DynaNail Hybrid

GUDID M97026010071300

DynaNail Hybrid, 7mm x 130mm

Medshape, Inc.

Arthrodesis nail, sterile
Primary Device IDM97026010071300
NIH Device Record Key5c2f4dbd-f388-4047-b97c-9911fb28607a
Commercial Distribution StatusIn Commercial Distribution
Brand NameDynaNail Hybrid
Version Model Number2601-00-7130
Company DUNS601306413
Company NameMedshape, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchfalse
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM97026010071300 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, Fixation, Bone

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-05-03
Device Publish Date2021-04-23

On-Brand Devices [DynaNail Hybrid]

M97026010071300DynaNail Hybrid, 7mm x 130mm
M97026010071200DynaNail Hybrid, 7mm x 120mm
M97026010071100DynaNail Hybrid, 7mm x 110mm
M97026010071000DynaNail Hybrid, 7mm x 100mm
M97026010070900DynaNail Hybrid, 7mm x 90mm
M97026010070800DynaNail Hybrid, 7mm x 80mm
M97026010070700DynaNail Hybrid, 7mm x 70mm
M97026010070600DynaNail Hybrid, 7mm x 60mm
M97026010071400DynaNail Hybrid, 7mm x 140mm

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