TransFasten-LSF, Implant Driver Shaft

GUDID M73910290050

Implant Driver Shaft

CAPTIVA SPINE, INC.

Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable Surgical screwdriver, reusable
Primary Device IDM73910290050
NIH Device Record Keyd59dd972-395f-444b-a24f-73b9bc7f8dc0
Commercial Distribution StatusIn Commercial Distribution
Brand NameTransFasten-LSF, Implant Driver Shaft
Version Model Number10-2-9005
Company DUNS836975784
Company NameCAPTIVA SPINE, 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

Customer Support Contacts

Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com
Phone561-277-9480
Emailinfo@captivaspine.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM73910290050 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

[M73910290050]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-05-03
Device Publish Date2024-04-25

Devices Manufactured by CAPTIVA SPINE, INC.

M739102900109 - TransFasten - LSF, General Instrument Tray2024-05-03 Sterilization Case - General Instrument Tray
M73910290020 - TransFasten - LSF, Quick Connect Drill2024-05-03 Quick Connect Drill
M73910290030 - TransFasten-LSF, Tissue Protector2024-05-03 Tissue Protector
M73910290050 - TransFasten-LSF, Implant Driver Shaft2024-05-03Implant Driver Shaft
M73910290050 - TransFasten-LSF, Implant Driver Shaft2024-05-03 Implant Driver Shaft
M73910290060 - TransFasten-LSF, Offset Guide2024-05-03 Offset Guide
M73910290070 - TransFasten-LSF, Tissue Dilator2024-05-03 Tissue Dilator
M739102901009 - TransFasten-LSF, Plunger Rod2024-05-03 Plunger Rod
M73910290110 - TransFasten - LSF, Implant Filling Tube2024-05-03 Implant Filling Tube
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