Maxim Tib Block with VG Feat SSI005899

GUDID 00889024589025

Zimmer, Inc.

Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable Orthopaedic prosthesis implantation instrument, reusable
Primary Device ID00889024589025
NIH Device Record Keybdac4cca-a6e6-409c-b123-a9396d540faf
Commercial Distribution StatusIn Commercial Distribution
Brand NameMaxim Tib Block with VG Feat
Version Model NumberSSI005899
Catalog NumberSSI005899
Company DUNS056038268
Company NameZimmer, Inc.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
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

Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com
Phone1 (800) 343-9500
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 Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]
GS100889024589025 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument
LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


[00889024589025]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2020-06-17
Device Publish Date2020-06-09

On-Brand Devices [Maxim Tib Block with VG Feat]

00889024589032SSI005900
00889024589025SSI005899

© 2020 FDA.report
This site is not affiliated with or endorsed by the FDA.