02-019-50-0002

GUDID 10885862286024

DISTAL CUT GUIDE

Exactech, Inc.

Osteotomy guide, reusable
Primary Device ID10885862286024
NIH Device Record Keyd529cefd-d909-42f0-8b7d-779acfc4d366
Commercial Distribution StatusIn Commercial Distribution
Version Model Number02-019-50-0002
Catalog Number02-019-50-0002
Company DUNS157565946
Company NameExactech, 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 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

Device Identifiers

Device Issuing AgencyDevice ID
GS110885862286024 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

JWHPROSTHESIS, KNEE, PATELLOFEMOROTIBIAL, SEMI-CONSTRAINED, CEMENTED, POLYMER/METAL/POLYMER

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


[10885862286024]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-05
Device Publish Date2022-07-28

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