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Trellis SI Joint Fusion System

FDA UDI

Class II (US FDA UDI)

by Orthofundamentals, Llc

Identity

Trade Name
Trellis SI Joint Fusion System FDA UDI
Generic Name
Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated FDA UDI
Device Name
11mm x 30mm Trellis SI Joint Fusion Screw FDA UDI
Model / Reference
OFSI1130 FDA UDI
Description
11mm x 30mm Trellis SI Joint Fusion Screw FDA UDI

Identifiers

Primary DI / UDI-DI
G204OFSI11300 FDA UDI
510(k) Number
K212962 FDA UDI
FDA Product Code
OUR FDA UDI
GMDN Term
Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3040 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

Yes

FDA UDI

Single Use

Yes

FDA UDI

Implantable

Yes

FDA UDI

Contains Latex

No

FDA UDI

Prescription Use

Yes

FDA UDI

Over-the-Counter

No

FDA UDI

Convenience Kit

No

FDA UDI

Combination Product

No

FDA UDI

HCT/P

No

FDA UDI

Premarket Exempt

No

FDA UDI

Lot / Batch Number

Yes

FDA UDI

Serial Number

No

FDA UDI

Expiration Date

Yes

FDA UDI

Manufacturing Date

No

FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 11 Millimeter FDA UDI
Length — 30 Millimeter FDA UDI

Category: Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated

Trellis SI Joint Fusion System by Orthofundamentals, Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sacroiliac joint transarticular fixation/arthrodesis implant, uncoated.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI efb17594-7bff-44bd-87d4-889445ac0fec 36 fields · synced Jun 6, 2026