PROGRESSIVE HIP SYSTEM 166328

GUDID 00880304258242

Biomet Orthopedics, LLC

Coated hip femur prosthesis, modular
Primary Device ID00880304258242
NIH Device Record Keyd9502439-3164-4f14-b69c-66283c05ce72
Commercial Distribution StatusIn Commercial Distribution
Brand NamePROGRESSIVE HIP SYSTEM
Version Model Number166328
Catalog Number166328
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
GS100880304258242 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MEHProsthesis, hip, semi-constrained, uncemented, metal/polymer, non-porous, calicum-phosphate

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-10-24

On-Brand Devices [PROGRESSIVE HIP SYSTEM]

00880304258273166331
00880304258266166330
00880304258259166329
00880304258242166328
00880304258235166327
00880304258228166326
00880304258211166325
00880304258204166324
00880304258181166323
00880304258174166322
00880304258167166321
00880304258150166320
00880304258143166319
00880304258136166318
00880304258129166317
00880304258112166316
00880304258105166315
00880304258082166314
00880304057418CP156642
00880304057401CP156641
00880304057395CP156640
00880304057340CP156526
00880304057333CP156525
00880304057326CP156524
00880304057319CP156523
00880304057302CP156522

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