Bone Clamp Ulnar Shortening

GUDID 00810054091806

Bone Clamp Ulnar Shortening

AVANTI ORTHOPAEDICS LLC

Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile Internal orthopaedic fixation system, plate/screw, non-bioabsorbable, non-sterile
Primary Device ID00810054091806
NIH Device Record Key83c32d1d-13f7-4b21-9136-1111685e6e48
Commercial Distribution StatusIn Commercial Distribution
Brand NameBone Clamp Ulnar Shortening
Version Model NumberBCUS
Company DUNS043505370
Company NameAVANTI ORTHOPAEDICS LLC
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 Usefalse
Lot Batchtrue
Serial Numberfalse
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com
Phone6103167345
Emailinfo@avantiortho.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100810054091806 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HRSPlate, Fixation, Bone

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


[00810054091806]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2021-12-16
Device Publish Date2021-12-08

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