MUSTmini OC pre-bent Rod

GUDID 07630030865145

MUST MINI OC pre-bent Rod 75° Ø3.5x 120mm (ste)

Medacta International SA

Bone-screw internal spinal fixation system, sterile
Primary Device ID07630030865145
NIH Device Record Keycf0bde5c-0e75-49a2-9927-a4c4dde50bea
Commercial Distribution StatusIn Commercial Distribution
Brand NameMUSTmini OC pre-bent Rod
Version Model Number03.75.624
Company DUNS488227125
Company NameMedacta International SA
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
GS107630030865145 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

NKGPosterior Cervical Screw System

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-11-02
Device Publish Date2021-10-25

On-Brand Devices [MUSTmini OC pre-bent Rod]

07630030865152MUST MINI OC pre-bent Rod 75° Ø3.5x 200mm (ste)
07630030865145MUST MINI OC pre-bent Rod 75° Ø3.5x 120mm (ste)
07630030865138MUST MINI OC pre-bent Rod 60° Ø3.5x 200mm (ste)
07630030865121MUST MINI OC pre-bent Rod 60° Ø3.5x 120mm (ste)
07630030865114MUST MINI OC pre-bent Rod 45° Ø3.5x 200mm (ste)
07630030865107MUST MINI OC pre-bent Rod 45° Ø3.5x 120mm (ste)

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