Screw, Cannulated 5.5x40mm, Full Thread 419-781

GUDID 00846468041366

Screw, Cannulated 5.5x40mm, Full Thread

Pioneer Surgical Technology, Inc.

Orthopaedic bone screw, non-bioabsorbable, non-sterile
Primary Device ID00846468041366
NIH Device Record Key55873cf2-078f-4eb9-b038-7fe28f2a7975
Commercial Distribution StatusIn Commercial Distribution
Brand NameScrew, Cannulated 5.5x40mm, Full Thread
Version Model Number419-781
Catalog Number419-781
Company DUNS793384496
Company NamePioneer Surgical Technology, Inc.
Device Count1
DM Exemptfalse
Pre-market Exemptfalse
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usetrue
Lot Batchtrue
Serial Numberfalse
Manufacturing Datefalse
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptiontrue
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com
Phone+1(906)226-9909
Emaillabeling@resolvesurg.com

Device Identifiers

Device Issuing AgencyDevice ID
GS100846468041366 [Primary]

FDA Pre-market Approvals/Notifications & deNovo

FDA Product Code

OURSacroiliac joint fixation

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


[00846468041366]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusUpdate
Device Record StatusPublished
Public Version Number3
Public Version Date2018-07-06
Device Publish Date2015-12-10

Devices Manufactured by Pioneer Surgical Technology, Inc.

00840298700028 - CODA™ Anterior Cervical Plate System2025-12-18 Modular Drill
00840298700110 - CODA™ Anterior Cervical Plate System2025-12-18 Modular Tap
00840298700677 - CODA™ Anterior Cervical Plate System2025-12-18 Driver, Threaded
00840298701957 - CODA™ Anterior Cervical Plate System2025-12-18 1 Level Template
00840298702022 - CODA™ Anterior Cervical Plate System2025-12-18 2 Level Template
00840298702251 - CODA™ Anterior Cervical Plate System2025-12-18 4 Level Template
00840298700608 - CODA™ Anterior Cervical Plate System2025-12-17 AO Handle
00840298700776 - CODA™ Anterior Cervical Plate System2025-12-17 Intradiscal Guide, 7mm/8mm

© 2025 FDA.report
This site is not affiliated with or endorsed by the FDA.