Implant Caddy

GUDID M739CP50901

SmartLOX Implant Caddy

CAPTIVA SPINE, INC.

Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable Instrument tray, reusable
Primary Device IDM739CP50901
NIH Device Record Keyd8b37243-8fad-4be0-bd57-76562d6e777b
Commercial Distribution StatusIn Commercial Distribution
Brand NameImplant Caddy
Version Model NumberCP50901
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 Batchfalse
Serial Numbertrue
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
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
HIBCCM739CP50901 [Primary]

FDA Product Code

FSMTray, Surgical, Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

[M739CP50901]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-10-09
Device Publish Date2023-09-29

On-Brand Devices [Implant Caddy]

M739FCT09010FCT0901
M739CP50901SmartLOX Implant Caddy
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