S³ KW20SS

GUDID 00887868443886

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 ID00887868443886
NIH Device Record Keye1799327-db97-489e-9537-8b9aa08f9cbe
Commercial Distribution StatusIn Commercial Distribution
Brand Name
Version Model NumberKW20SS
Catalog NumberKW20SS
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 Datefalse
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
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [Primary]
GS100887868443886 [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 Usetrue
Device Is Sterilefalse

[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


[00887868443886]

Moist Heat or Steam Sterilization


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 [S³]

008878684527892312-01-310
00887868443886KW20SS

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