JuggerKnot Short Rigid Reusable Guide SSI003516

GUDID 00889024664739

Biomet Orthopedics, LLC

Orthopaedic implantation sleeve, reusable
Primary Device ID00889024664739
NIH Device Record Key42a2aa47-29d6-4009-bafe-3c5be911bef0
Commercial Distribution StatusIn Commercial Distribution
Brand NameJuggerKnot Short Rigid Reusable Guide
Version Model NumberSSI003516
Catalog NumberSSI003516
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 Usefalse
Lot Batchtrue
Serial Numberfalse
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

Device Dimensions

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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
GS100889024664739 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

MBIFastener, Fixation, Nondegradable, Soft Tissue

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


[00889024664739]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-29
Device Publish Date2024-07-19

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08428898885691 - BIPASS DISPOSABLE PUSHER2024-09-11
00880304338548 - AGC ANTERIOR FILE2024-09-11
00880304339224 - PARALLEL PULLER2024-09-11
00880304342187 - AGC MODULAR TIBIAL II2024-09-11
00880304365247 - BIO-MODULAR2024-09-11

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