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Extension Cap

FDA UDI

Class I (US FDA UDI)

by OsteoCentric Technologies, Inc

Identity

Trade Name
EXTENSION CAP FDA UDI
Generic Name
Orthopaedic instrument surgical connector FDA UDI
Device Name
EXTENSION CAP FDA UDI
Model / Reference
101-0018 FDA UDI
Description
EXTENSION CAP FDA UDI

Identifiers

Catalog Number
101-0018 FDA UDI
Primary DI / UDI-DI
00810097802339 FDA UDI
510(k) Number
K221332 FDA UDI
FDA Product Code
FZX FDA UDI
GMDN Term
Orthopaedic instrument surgical connector FDA UDI

Classification

Device Class
Class I FDA UDI
Regulation Number
878.4800 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

Category: Orthopaedic instrument surgical connector

Extension Cap by OsteoCentric Technologies, Inc — Class I — 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 4410bf7f-49aa-4767-839f-cc6af31c99d3 36 fields · synced May 29, 2026