01-007-04-3230

GUDID 10885862552952

ART DRILL DRVR, 3.2X30MM

Exactech, Inc.

Fluted surgical drill bit, reusable
Primary Device ID10885862552952
NIH Device Record Keyc5eb0c21-d23b-47f4-9d40-215a8ce618a2
Commercial Distribution StatusIn Commercial Distribution
Version Model Number01-007-04-3230
Catalog Number01-007-04-3230
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 Dimensions

Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0
Device Size Text, specify0
Outer Diameter3.2 Millimeter
Length30 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110885862552952 [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

[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


[10885862552952]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-08-26
Device Publish Date2022-08-18

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10885862653307 - Truliant2025-01-16 Special Universal Baseplate Tibial Trial, Size 5
10885862653321 - Truliant2025-01-16 Special Universal Baseplate Tibial Trial, Size 1.5
10885862653338 - Truliant2025-01-16 Special Universal Baseplate Tibial Trial, Size 2.5
10885862653345 - Truliant2025-01-16 Special Universal Baseplate Tibial Trial, Size 3.5

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