TransFasten

GUDID M7399851402290

Marking Pin, 229mm, Non-Threaded Trocar, Blunt, SS

CAPTIVA SPINE, INC.

Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use Intraoperative orthopaedic bone pin/screw, single-use
Primary Device IDM7399851402290
NIH Device Record Keybec3569a-30b0-491d-98e6-632b8d12db08
Commercial Distribution StatusIn Commercial Distribution
Brand NameTransFasten
Version Model Number98514-0229
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 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

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 Dimensions

Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter
Length229 Millimeter

Device Identifiers

Device Issuing AgencyDevice ID
HIBCCM7399851402290 [Primary]

FDA Product Code

LXHOrthopedic Manual Surgical Instrument

Sterilization

Steralize Prior To Usetrue
Device Is Sterilefalse

[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


[M7399851402290]

Moist Heat or Steam Sterilization


Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-08-24
Device Publish Date2023-08-16

On-Brand Devices [TransFasten]

M7399851422030Marking Pin, 203mm, Conical Blunt, SS
M7399851412030Marking Pin, 203mm, Double Blunt, SS
M7399851402030Marking Pin, 203mm, NonThreaded, SS
M7399851472290Marking Pin, 229mm, Blunt, SS
M7399851462290Marking Pin, 229mm, Non-Threaded Trocar, Blunt, SS
M7399851452290Marking Pin, 229mm, Conical Blunt, SS
M7399851443050Marking Pin, 305mm, Conical Blunt, SS
M7399851442290Marking Pin, 229mm, Blunt, SS
M7399851432290Marking Pin, 229mm, Non-Threaded Trocar, Blunt, SS
M7399851422290Marking Pin, 229mm, Conical Blunt, SS
M7399851412290Marking Pin, 229mm, Double Blunt, SS
M7399851402290Marking Pin, 229mm, Non-Threaded Trocar, Blunt, SS
M739985222229LD (.125” Wire) Marking Pin, 229mm, Conical Blunt
M739985221305LD (.125” Wire) Marking Pin, 305mm, Non-Threaded Trocar
M739985221229LD (.125” Wire) Marking Pin, 229mm, Non-Threaded Trocar

Trademark Results [TransFasten]

Mark Image

Registration | Serial
Company
Trademark
Application Date
TRANSFASTEN
TRANSFASTEN
86538411 5443633 Live/Registered
Captiva Spine, Inc.
2015-02-18

© 2024 FDA.report
This site is not affiliated with or endorsed by the FDA.