FDA.reportPublic FDA data

BowTie SI Fusion System

Primary DI
00850053568558
Brand
BowTie SI Fusion System
Company
SAIL FUSION, LLC
Model
90-JFB-100300
Device description
Guidewire, Long
Published
2025-01-27
Public version status
New
Distribution status
In Commercial Distribution
MRI safety
Labeling does not contain MRI Safety Information

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
00850053568558PrimaryGS10

Alternate GTIN / UPC / EAN Codes

Source identifier, GTIN-14 normalized, UPC-A table
Source identifierGTIN-14 normalizedUPC-AEAN-13
00850053568558008500535685588500535685580850053568558

GMDN Terms#

Term, Definition table
TermDefinition
Sacroiliac joint transarticular fixation/arthrodesis implantation kitA collection of surgical instruments and devices intended to be used for the implantation of a sacroiliac joint transarticular fixation/arthrodesis implant during a minimally-invasive procedure. It typically consists of a tray, dedicated soft-tissue protectors, depth gauges, pin sleeves, drill sleeves, drill bits, broaches, a parallel pin guide, handles, slide hammer shafts, impactors, and a removal/adaptor tool; the implant(s) is not included. This is a reusable device.

Sterilization Methods#

Method table
Method
Moist Heat or Steam Sterilization

Regulatory Flags#

DUNS number
118308843
Device count
1
Premarket exempt
true
Lot or batch
true
Manufacturing date on label
true
Sterilization required before use
true

Other Devices From This Company#

Primary DI, Brand, Model table
Primary DIBrandModelCatalogPublished
00850053568565BowTie SI Fusion System90-JFB-2003002025-01-31
00850053568572BowTie SI Fusion SystemPKG-90-JFA-2000452025-01-31
00850053568589BowTie SI Fusion SystemPKG-90-JFA-2000502025-01-27
00850053568008BowTie SI Fusion System90-JFA-1000302024-05-24
00850053568015BowTie SI Fusion System90-JFA-1000352024-05-24
00850053568022BowTie SI Fusion System90-JFA-1000402024-05-24
00850053568039BowTie SI Fusion System90-JFA-1000452024-05-24
00850053568046BowTie SI Fusion System90-JFA-1000502024-05-24
00850053568053BowTie SI Fusion System90-JFA-1050302024-05-24
00850053568060BowTie SI Fusion System90-JFA-1050352024-05-24
00850053568077BowTie SI Fusion System90-JFA-1050402024-05-24
00850053568084BowTie SI Fusion System90-JFA-1050452024-05-24
00850053568091BowTie SI Fusion System90-JFA-1050502024-05-24
00850053568107BowTie SI Fusion System90-JFA-2000552024-05-24
00850053568114BowTie SI Fusion System90-JFA-2000602024-05-24
00850053568121BowTie SI Fusion System90-JFA-2000652024-05-24
00850053568138BowTie SI Fusion System90-JFA-2000702024-05-24
00850053568145BowTie SI Fusion System90-JFA-2000752024-05-24
00850053568152BowTie SI Fusion System90-JFA-2000802024-05-24
00850053568169BowTie SI Fusion System90-JFA-2000852024-05-24

Other Devices Sharing Product Codes#

Primary DI, Brand, Company table
Primary DIBrandCompanyProduct codePublished
00888867550292Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550308Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550315Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550322Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550339Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550346Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550353Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550360Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550377Arthrex®ARTHREX, INC.LXH2026-09-18
00888867550384Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552692Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552708Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552715Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552722Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552739Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552746Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552753Arthrex®ARTHREX, INC.LXH2026-09-18
00888867552760Arthrex®ARTHREX, INC.LXH2026-09-18
00888867574564Arthrex®ARTHREX, INC.LXH2026-09-18
00888867574571Arthrex®ARTHREX, INC.LXH2026-09-18
00888867574588Arthrex®ARTHREX, INC.LXH2026-09-18
04054896000831Control GaugesSilony Medical GmbHLXH2026-09-18
04054896000855Implant ModifierSilony Medical GmbHLXH2026-09-18
04054896000862Implant ModifierSilony Medical GmbHLXH2026-09-18
04054896000879Implant ModifierSilony Medical GmbHLXH2026-09-18
04054896000886Forceps and ClampsSilony Medical GmbHLXH2026-09-18
04054896000893(Re-) Positioning ToolsSilony Medical GmbHLXH2026-09-18
04054896000909(Re-) Positioning ToolsSilony Medical GmbHLXH2026-09-18
04054896000916(Re-) Positioning ToolsSilony Medical GmbHLXH2026-09-18
04054896000923AdapterSilony Medical GmbHLXH2026-09-18