OSS™ Orthopedic Salvage System 151869

GUDID 00887868267239

Biomet Orthopedics, LLC

Femur/tibia shaft prosthesis
Primary Device ID00887868267239
NIH Device Record Key6ff473c7-7615-432d-80d7-768dc39b13f4
Commercial Distribution StatusIn Commercial Distribution
Brand NameOSS™ Orthopedic Salvage System
Version Model Number151869
Catalog Number151869
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

Device Dimensions

Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100887868267239 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JDIProsthesis, hip, semi-constrained, metal/polymer, cemented

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-04-27
Device Publish Date2018-11-13

On-Brand Devices [OSS™ Orthopedic Salvage System]

00887868267253151871
00887868267246151870
00887868267239151869
00887868267222151868
00887868267215151867
00887868267208151866
00887868267192151865
00887868267185151864
00887868267178151863
00887868267161151862
00887868267154151861
00887868251856CP102848
00887868251849CP102847
00887868251832CP102846
00887868251825CP102845
00887868251818CP102844
00887868251801CP102843
00887868251795CP102840
00887868251788CP102839
00887868251771CP102838

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