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Nebula High Offset Size 6

FDA UDI

Class II (US FDA UDI)

by Signature Orthopaedics Pty Ltd

Identity

Trade Name
Nebula High Offset Size 6 FDA UDI
Generic Name
Coated hip femur prosthesis, modular FDA UDI
Model / Reference
111-59-0106 FDA UDI

Identifiers

Primary DI / UDI-DI
09348215134709 FDA UDI
510(k) Number
K243029 FDA UDI
FDA Product Code
MEH FDA UDI
OQI FDA UDI
LPH FDA UDI
OQG FDA UDI
KWZ FDA UDI
KWL FDA UDI
KWY FDA UDI
LZO FDA UDI
GMDN Term
Coated hip femur prosthesis, modular FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3353 FDA UDI
888.3358 FDA UDI
888.3310 FDA UDI
888.3360 FDA UDI
888.3390 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

Yes

FDA UDI

Category: Coated hip femur prosthesis, modular

Nebula High Offset Size 6 by Signature Orthopaedics Pty Ltd — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Coated hip femur prosthesis, modular.

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 ae333d6f-f167-4bd4-a075-572427bf0f45 33 fields · synced Jun 8, 2026