4-Hole Drill Guide

GUDID M739203000210

4-Hole LD Drill Guide

CAPTIVA SPINE, INC.

Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable Surgical drill guide, reusable
Primary Device IDM739203000210
NIH Device Record Key5e57aadd-8270-4fb0-bffb-e1a7b0176a1f
Commercial Distribution StatusIn Commercial Distribution
Brand Name4-Hole Drill Guide
Version Model Number20300-0210
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
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
HIBCCM739203000210 [Primary]

FDA Product Code

HXYBrace, Drill

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

[M739203000210]

Moist Heat or Steam Sterilization

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-03-19
Device Publish Date2024-03-11

On-Brand Devices [4-Hole Drill Guide]

M739203000200020300-0200
M739203000200N04-Hole Drill Guide for NAV
M7392030002104-Hole LD Drill Guide
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