Modular Arthrodesis Nail CP260610

GUDID 00889024703193

Biomet Orthopedics, LLC

Knee arthroplasty wedge
Primary Device ID00889024703193
NIH Device Record Key4f9d6639-e42f-4af8-ba03-4970251692a3
Commercial Distribution StatusIn Commercial Distribution
Brand NameModular Arthrodesis Nail
Version Model NumberCP260610
Catalog NumberCP260610
Company DUNS129278169
Company NameBiomet Orthopedics, LLC
Device Count1
DM Exempttrue
Pre-market Exemptfalse
MRI Safety StatusMR Unsafe
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

Device Dimensions

Device Size Text, specify0
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Device Identifiers

Device Issuing AgencyDevice ID
GS100889024703193 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

HSBROD, FIXATION, INTRAMEDULLARY AND ACCESSORIES

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2025-12-10
Device Publish Date2025-12-02

On-Brand Devices [Modular Arthrodesis Nail]

00880304083073CP260610
00880304083066CP260609
00880304083059CP260608
00880304083042CP260607
00880304083035CP260606
00880304083028CP260605
00880304083011CP260604
00880304083004CP260603
00880304082991CP260602
00880304082984CP260601
00880304082977CP260600
00889024703254CP260609
00889024703230CP260604
00889024703216CP260600
00889024703209CP260603
00889024703193CP260610

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