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NovoHip Total Hip System

FDA UDI

Class II (US FDA UDI)

by Novosource, Inc.

Identity

Trade Name
NovoHip Total Hip System FDA UDI
Generic Name
Press-fit hip femur prosthesis, one-piece FDA UDI
Device Name
Taper Stem, Std Offset Sz 9 FDA UDI
Model / Reference
1100-0009 FDA UDI
Description
Taper Stem, Std Offset Sz 9 FDA UDI

Identifiers

Catalog Number
1100-0009 FDA UDI
Primary DI / UDI-DI
00811382038082 FDA UDI
510(k) Number
K132158 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
GMDN Term
Press-fit hip femur prosthesis, one-piece FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3358 FDA UDI
888.3353 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
Length — 98 Millimeter FDA UDI

Category: Press-fit hip femur prosthesis, one-piece

NovoHip Total Hip System by Novosource, Inc. — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit hip femur prosthesis, one-piece.

Cleared under the same submission

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Novosource, Inc.

Sources (1)

  • FDA UDI 75bed002-3c50-4094-a509-035550edb21b 37 fields · synced Jun 6, 2026