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iNSitu Total Hip System

FDA UDI

Class II (US FDA UDI)

by Nextstep Arthropedix

Identity

Trade Name
iNSitu Total Hip System FDA UDI
Generic Name
Coated femoral stem prosthesis, modular FDA UDI
Device Name
Femoral Stem, Size 11, Lateral, Taper Coated FDA UDI
Model / Reference
10-11-0011-TC FDA UDI
Description
Femoral Stem, Size 11, Lateral, Taper Coated FDA UDI

Identifiers

Primary DI / UDI-DI
00816127029158 FDA UDI
FDA Product Code
LPH FDA UDI
LZO FDA UDI
OQG FDA UDI
OQI FDA UDI
GMDN Term
Coated femoral stem 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
Sterilization Method
Ethylene Oxide FDA UDI

Category: Coated femoral stem prosthesis, modular

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

Similar devices

Also classified as Coated femoral stem prosthesis, modular.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Sources (1)

  • FDA UDI 25aeba92-9780-4ef5-a2e6-b378448397c2 33 fields · synced Jun 8, 2026