FDA.reportPublic FDA data

ZAVATION GUIDE WIRE

Primary DI
00197157015015
Brand
ZAVATION GUIDE WIRE
Company
Zavation LLC
Model
989-1009-4
Device description
GUIDE WIRE, 610mm NITINOL, BLUNT TIP
Published
2025-06-03
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

Premarket Submissions#

Submission, Supplement table
SubmissionSupplement
K243908000

Premarket Details#

Submission, Supplement, Device table
SubmissionSupplementDeviceApplicantDecision dateProduct code
K243908000Tiger 2 SystemZavation Medical Products, LLC2025-02-03NKB

Identifiers And Packaging#

Identifier, Type, Agency table
IdentifierTypeAgencyPackage quantityStatus
00197157015015PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00197157015015001971570150151971570150150197157015015

GMDN Terms#

Term, Definition table
TermDefinition
Orthopaedic bone pin, non-bioabsorbableA thin, implantable rod intended to be used for the stabilization of a bone fracture or bone grafts, or for an osteotomy or arthrodesis. It is typically drilled into bone and may be smooth or threaded, solid or cannulated, and/or semi-flexible. Also known as a K-Wire, it may in addition be intended to assist with the introduction of a surgical instrument and/or implant; it is not intended for implantation into the intramedullary canal (i.e., not a nail). It is made of a material that is not chemically degraded or absorbed by natural body processes (e.g., stainless steel). Some designs may have a break-off shank and/or be coated to improve long-term fixation. This is a single-use device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Contacts#

Phone, Email table
PhoneEmail
6019191119info@zavation.com

Regulatory Flags#

DUNS number
069472800
Device count
1
Lot or batch
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00197157075989ZAVATION DISTRACTORZAV-1395-072026-05-28
00197157075996ZAVATION DISTRACTORZAV-1395-082026-05-28
00197157076009ZAVATION DISTRACTORZAV-1395-092026-05-28
00197157076016ZAVATION DISTRACTORZAV-1395-102026-05-28
00197157076023ZAVATION DISTRACTORZAV-1395-112026-05-28
00197157076030ZAVATION DISTRACTORZAV-1395-122026-05-28
00197157076047ZAVATION DISTRACTORZAV-1395-132026-05-28
00197157076054ZAVATION DISTRACTORZAV-1395-142026-05-28
00197157076061ZAVATION DISTRACTORZAV-1395-152026-05-28
00197157075835ZAVATION DRIVERZAV-13982026-05-27
00197157075842ZAVATION K-WIREZAV-13972026-05-27
00197157075859ZAVATION INSERTERZAV-10552026-05-27
00197157068332ZAVATION INSTRUMENT TRAY14T009142026-05-20
00197157068349ZAVATION INSTRUMENT TRAY14T009152026-05-20
00197157068356ZAVATION INSTRUMENT TRAY14T009162026-05-20
00197157068363ZAVATION INSTRUMENT TRAY14T009172026-05-20
00197157068370ZAVATION INSTRUMENT TRAY14T009192026-05-20
00197157068387ZAVATION INSTRUMENT TRAY14T009202026-05-20
00197157068394ZAVATION INSTRUMENT TRAY14T009212026-05-20
00197157068400ZAVATION INSTRUMENT TRAY14T009222026-05-20

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Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
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