10/4 PSN TIBIA STYLUS SSI008071

GUDID 00889024685611

Zimmer, Inc.

Orthopaedic prosthesis implantation positioning instrument, reusable
Primary Device ID00889024685611
NIH Device Record Key737b1711-4168-4b27-83a4-ab55e2592e4b
Commercial Distribution StatusIn Commercial Distribution
Brand Name10/4 PSN TIBIA STYLUS
Version Model NumberSSI008071
Catalog NumberSSI008071
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

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 Identifiers

Device Issuing AgencyDevice ID
GS100889024685611 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


[00889024685611]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-01-21
Device Publish Date2025-01-13

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00889024658165 - Persona® Knee System2025-02-14
00889024658172 - Persona® Knee System2025-02-14
00889024658189 - Persona® Knee System2025-02-14
00889024658196 - Persona® Knee System2025-02-14
00889024658202 - Persona® Knee System2025-02-14

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