VT4.5L22

GUDID 03700569606398

NEWCLIP TECHNICS

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID03700569606398
NIH Device Record Key5b6fb4dc-e2d4-42d1-9468-8bf78a6672fa
Commercial Distribution StatusIn Commercial Distribution
Version Model NumberVT4.5L22
Catalog NumberVT4.5L22
Company DUNS263281904
Company NameNEWCLIP TECHNICS
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
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
GS103700569606398 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, Fixation, Bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[03700569606398]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number4
Public Version Date2024-02-19
Device Publish Date2016-09-26

Devices Manufactured by NEWCLIP TECHNICS

03700569602475 - Activmotion2024-11-21
03700569602499 - Activmotion2024-11-21
03700569607586 - Alians Clavicle2024-11-21
03700569607609 - Alians Clavicle2024-11-21
03700569608958 - Alians Clavicle2024-11-21
03700569608972 - Alians Clavicle2024-11-21
03700569608989 - Alians Clavicle2024-11-21
03700569608996 - Alians Clavicle2024-11-21

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.