MAX VPC™ 133211105

GUDID 00887868445248

Biomet Orthopedics, LLC

Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire Orthopaedic bone wire
Primary Device ID00887868445248
NIH Device Record Key24ff33e9-4a9a-4aee-8b06-a71f756c7dc8
Commercial Distribution StatusIn Commercial Distribution
Brand NameMAX VPC™
Version Model Number133211105
Catalog Number133211105
Company DUNS129278169
Company NameBiomet Orthopedics, 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 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

Customer Support Contacts

Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com
Phone+1(800)348-9500
Emailcustomerservice@zimmerbiomet.com

Device Dimensions

Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]
GS100887868445248 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
HWCScrew, fixation, bone
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 Date2020-09-14
Device Publish Date2020-09-04

On-Brand Devices [MAX VPC™]

00887868337482231201440
00887868337475231201430
00887868337468231201425
00887868445255133214127
00887868445248133211105
00887868445231133209095

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