181-00-06

GUDID 10885862241535

DRILL GUIDE, 3.2mm

Exactech, Inc.

Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine Surgical guillotine
Primary Device ID10885862241535
NIH Device Record Key3700f358-f1a3-4524-a899-b1617265989b
Commercial Distribution StatusIn Commercial Distribution
Version Model Number181-00-06
Catalog Number181-00-06
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

Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0
Lumen/Inner Diameter3.2 Millimeter
Device Size Text, specify0

Device Identifiers

Device Issuing AgencyDevice ID
GS110885862241535 [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

[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


[10885862241535]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2022-10-12
Device Publish Date2022-10-04

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10885862628947 - EXACTECHGPS2024-04-15 Station V3

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