Threaded Knob SSI005895

GUDID 00889024588981

Zimmer, Inc.

Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable Bone-coring punch, reusable
Primary Device ID00889024588981
NIH Device Record Key3006c1ce-57a9-467d-8d31-373809df9122
Commercial Distribution StatusIn Commercial Distribution
Brand NameThreaded Knob
Version Model NumberSSI005895
Catalog NumberSSI005895
Company DUNS056038268
Company NameZimmer, Inc.
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 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
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
Phone1 (800) 343-9500
Emailcustomerservice@zimmerbiomet.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100889024588981 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

KWSProsthesis, Shoulder, Semi-Constrained, Metal/Polymer Cemented

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

Moist Heat or Steam Sterilization


[00889024588981]

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

Devices Manufactured by Zimmer, Inc.

00889024660595 - BIOMET Anterior Adapter2024-04-23
00889024660601 - BIOMET Posterior Adapter2024-04-23
00889024660816 - +9MM Spacer Block C/D 10mm 2024-04-23
00889024660823 - +9MM Spacer Block C/D 12mm 2024-04-23
00889024660830 - +9MM Spacer Block C/D 14mm 2024-04-23
00889024660847 - +9MM Spacer Block C/D 16mm 2024-04-23
00889024660854 - +9MM Spacer Block C/D 18mm 2024-04-23
00889024660861 - +9MM Spacer Block C/D 20mm 2024-04-23

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