Multi-Directional Tibial Tubercle Transfer System 23-800-1001

GUDID 00818720011899

Primary Guide

Kinamed, Inc.

Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable Orthopaedic surgical procedure kit, non-medicated, reusable
Primary Device ID00818720011899
NIH Device Record Key3ad4b059-84f5-4135-9a7d-7c0c10240a05
Commercial Distribution StatusIn Commercial Distribution
Brand NameMulti-Directional Tibial Tubercle Transfer System
Version Model Number23-800-1001
Catalog Number23-800-1001
Company DUNS184896645
Company NameKinamed, Inc.
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 Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Device Identifiers

Device Issuing AgencyDevice ID
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]
GS100818720011899 [Primary]

FDA Product Code

LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


[00818720011899]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number2
Public Version Date2020-06-23
Device Publish Date2020-06-05

On-Brand Devices [Multi-Directional Tibial Tubercle Transfer System]

00818720011899Primary Guide
00818720011905Drill Sleeve, 3.2mm
00818720012476Steinmann Pin , 2.4mm

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