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InSitu Hip System

FDA UDI

Class II (US FDA UDI)

by Nextstep Arthropedix

Identity

Trade Name
InSitu Hip System FDA UDI
Generic Name
Press-fit hip femur prosthesis, modular FDA UDI
Device Name
Femoral Stem, Size 7, Standard FDA UDI
Model / Reference
10-10-0007 FDA UDI
Description
Femoral Stem, Size 7, Standard FDA UDI

Identifiers

Catalog Number
10-10-0007 FDA UDI
Primary DI / UDI-DI
00816127022005 FDA UDI
510(k) Number
K161184 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
OQG FDA UDI
OQI FDA UDI
GMDN Term
Press-fit hip femur prosthesis, modular 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

Yes

FDA UDI

Dimensions & Sizes

Size
Length — 127 Millimeter FDA UDI

Category: Press-fit hip femur prosthesis, modular

InSitu Hip System by Nextstep Arthropedix — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Press-fit 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 134f021a-96ba-4fd7-bff1-5f1940e77056 37 fields · synced Jun 1, 2026