8203236000

GUDID 07613327304381

Single Trigger Large Collet 3.0 ? 4.2mm

STRYKER CORPORATION

Wire-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment Pin-driving power tool attachment
Primary Device ID07613327304381
NIH Device Record Key9309b13e-671c-49b5-bd7e-44bb229a7fbe
Commercial Distribution StatusIn Commercial Distribution
Version Model Number8203236000
Catalog Number8203236000
Company DUNS196548481
Company NameSTRYKER CORPORATION
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
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

Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com
Phone+1(800)253-3210
EmailInst.Stryker.cs@Stryker.com

Device Identifiers

Device Issuing AgencyDevice ID
GS107613327304381 [Primary]

FDA Product Code

HWEINSTRUMENT, SURGICAL, ORTHOPEDIC, AC-POWERED MOTOR AND ACCESSORY/ATTACHMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


[07613327304381]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2018-10-25
Device Publish Date2018-09-24

Devices Manufactured by STRYKER CORPORATION

07613327627664 - KNOTILUS+2024-03-15 2.9X12.5MM KNOTILUS+ HIP ANCHOR - PEEK
07613327627701 - KNOTILUS+2024-03-15 2.4X8.9MM KNOTILUS+ HIP ANCHOR - PEEK
07613327623796 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HIP
07613327623833 - KNOTILUS+2024-03-13 2.4X8.9MM DRILL, HARD BONE, HIP
07613327634686 - Iconix2024-03-12 Iconix DC Guide for 1.4mm anchor
07613327634693 - Iconix2024-03-12
07613327616675 - SPY2024-03-06
07613327616682 - SPY2024-03-06

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