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4.0mm Drill Bit Cann Hud-Mod

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
4.0mm Drill Bit Cann Hud-Mod FDA UDI
Generic Name
Sacroiliac joint transarticular fixation/arthrodesis implantation kit FDA UDI
Device Name
4.0mm Drill Bit Cann Hud-Mod FDA UDI
Model / Reference
202-80400 FDA UDI
Description
4.0mm Drill Bit Cann Hud-Mod FDA UDI

Identifiers

Catalog Number
202-80400 FDA UDI
Primary DI / UDI-DI
00810097800984 FDA UDI
510(k) Number
K230226 FDA UDI
FDA Product Code
HTW FDA UDI
GMDN Term
Sacroiliac joint transarticular fixation/arthrodesis implantation kit FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
888.4540 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

Yes

FDA UDI

Implantable

No

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

No

FDA UDI

Manufacturing Date

No

FDA UDI
Sterilization Method
Moist Heat or Steam Sterilization FDA UDI

Dimensions & Sizes

Size
Outer Diameter — 4.0 Millimeter FDA UDI

Category: Sacroiliac joint transarticular fixation/arthrodesis implantation kit

4.0mm Drill Bit Cann Hud-Mod by OsteoCentric Technologies, Inc — Class I — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Sacroiliac joint transarticular fixation/arthrodesis implantation kit.

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 4695605d-05b1-411c-81d9-4a5e91b6d939 37 fields · synced Jun 8, 2026