CAPTURE Facet Screw Set System 315-0015

GUDID M7403150015

Capture Drill

SPINEOLOGY INC.

Surgical drill guide, single-use
Primary Device IDM7403150015
NIH Device Record Keyfccf8470-727c-4ef5-8b9f-7f3968a2474c
Commercial Distribution StatusIn Commercial Distribution
Brand NameCAPTURE Facet Screw Set System
Version Model Number70-02-008-2
Catalog Number315-0015
Company DUNS033014361
Company NameSPINEOLOGY INC.
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusMR Unsafe
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datetrue
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com
Phone651-256-8500
Emailinfo@spineology.com

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7403150015 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usefalse
Device Is Steriletrue

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2024-07-24
Device Publish Date2024-07-16

On-Brand Devices [CAPTURE Facet Screw Set System]

M7404300032Graft Spacer
M7404300031Rasp
M7404300030Dilator
M7404300029EMG Cannula
M7404300028Screw Remover
M7404300027Cannula cleaner
M7404300026Driver Cannula
M7404300025Driver Shaft
M7404300024Tap
M7404300023Drill Guide
M7403150015Capture Drill

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