FDA.reportPublic FDA data

Cannulated Screw System +

Primary DI
00810040684180
Brand
Cannulated Screw System +
Company
Tyber Medical, LLC
Model
03.333.016.04
Catalog number
03.333.016.04
Device description
2.8MM THREADED GUIDE WIRE 450MM LENGTH/4 PACK
Published
2020-09-05
Public version status
Update
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information
Rx
true
Single use
true

Contact Domains#

Product Codes#

Code, Name table
CodeName
LXHORTHOPEDIC MANUAL SURGICAL INSTRUMENT

Product Code Classifications#

Code, Device, Specialty table
CodeDeviceSpecialtyClass
LXHOrthopedic Manual Surgical InstrumentOrthopedic1

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00810040684180PrimaryGS10
00810040684357Unit of UseGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00810040684180008100406841808100406841800810040684180
00810040684357008100406843578100406843570810040684357

GMDN Terms#

Term, Definition table
TermDefinition
Surgical drill guide, single-useA hand-held tubular surgical device designed to simultaneously place, angle, and guide a rotating surgical drill on hard tissue (e.g., bone), and to protect the surrounding soft tissue while the drill is in operation. It may have serrations at its distal end to enable firm placement on hard tissue surfaces (it is not bored into the tissue); it can have a handle at its proximal end for holding and manipulation, or it may be held by another device (e.g., orthopaedic jig). The device is typically dedicated to drill bit size, made of metal, and may have graduations along its length; it is not custom-made for a specific patient. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
+1(866)761-0933jstigliano@tybermed.com

Regulatory Flags#

DUNS number
010968002
Device count
4
Premarket exempt
true
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00196449033393A.L.P.S. mvX™7701030902026-07-23
00196449033409A.L.P.S. mvX™7701070902026-07-23
00196449011735A.L.P.S. mvX™7703000407703000402024-01-20
00196449011742A.L.P.S. mvX™7703000457703000452024-01-20
00196449011759A.L.P.S. mvX™7703000507703000502024-01-20
00196449011766A.L.P.S. mvX™7703000557703000552024-01-20
00196449011773A.L.P.S. mvX™7703000607703000602024-01-20
00196449011780A.L.P.S. mvX™7703000707703000702024-01-20
00196449011797A.L.P.S. mvX™7703520407703520402024-01-20
00196449011803A.L.P.S. mvX™7703520457703520452024-01-20
00196449011810A.L.P.S. mvX™7703520507703520502024-01-20
00196449011827A.L.P.S. mvX™7703520557703520552024-01-20
00196449011834A.L.P.S. mvX™7703520607703520602024-01-20
00196449011841A.L.P.S. mvX™7703520707703520702024-01-20
00196449011858A.L.P.S. mvX™7704010407704010402024-01-20
00196449011865A.L.P.S. mvX™7704010457704010452024-01-20
00196449011872A.L.P.S. mvX™7704010507704010502024-01-20
00196449011889A.L.P.S. mvX™7704010557704010552024-01-20
00196449011896A.L.P.S. mvX™7704010607704010602024-01-20
00196449011902A.L.P.S. mvX™7704010707704010702024-01-20

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00840314263636gSourceGSOURCE LLCLXH2026-07-17
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00840314264268gSourceGSOURCE LLCLXH2026-07-17
00840314264404gSourceGSOURCE LLCLXH2026-07-17
00840314264473gSourceGSOURCE LLCLXH2026-07-17