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5.5 x 150mm CURVED ROD

FDA UDI

Class II (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
5.5 x 150mm CURVED ROD FDA UDI
Generic Name
Orthopaedic instrument surgical connector FDA UDI
Device Name
5.5 x 150mm CURVED ROD FDA UDI
Model / Reference
101-10150 FDA UDI
Description
5.5 x 150mm CURVED ROD FDA UDI

Identifiers

Catalog Number
101-10150 FDA UDI
Primary DI / UDI-DI
00810097802735 FDA UDI
510(k) Number
K221332 FDA UDI
FDA Product Code
NKB FDA UDI
GMDN Term
Orthopaedic instrument surgical connector FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3070 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 — 5.5 Millimeter FDA UDI
Length — 150 Millimeter FDA UDI

Category: Orthopaedic instrument surgical connector

5.5 x 150mm CURVED ROD by OsteoCentric Technologies, Inc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Orthopaedic instrument surgical connector.

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 3bc9e731-86e4-461d-b207-ca8b6e078c2c 37 fields · synced Jun 8, 2026