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Responsive Orthopedics Total Knee Arthroplasty System

FDA UDI

Class II (US FDA UDI)

by Responsive Orthopedics Llc

Identity

Trade Name
Responsive Orthopedics Total Knee Arthroplasty System FDA UDI
Generic Name
Knee tibia prosthesis trial, reusable FDA UDI
Device Name
TRIAL 90-SRK-191216 POLY-MPCS 2X16 RIGHT FDA UDI
Model / Reference
90-SRK-191216 FDA UDI
Description
TRIAL 90-SRK-191216 POLY-MPCS 2X16 RIGHT FDA UDI

Identifiers

Catalog Number
90-SRK-191216 FDA UDI
Primary DI / UDI-DI
00841973107644 FDA UDI
FDA Product Code
JWH FDA UDI
GMDN Term
Knee tibia prosthesis trial, reusable FDA UDI

Classification

Device Class
Class II FDA UDI
Regulation Number
888.3560 FDA UDI
Commercial Distribution
In Commercial Distribution FDA UDI

Clinical & Handling

Sterile

No

FDA UDI

Single Use

No

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: Knee tibia prosthesis trial, reusable

Responsive Orthopedics Total Knee Arthroplasty System by Responsive Orthopedics Llc — Class II — FDA UDI — listed in FDA GUDID — regulatory data on deviCERTS

Similar devices

Also classified as Knee tibia prosthesis trial, reusable.

Authorization Coverage (1 country)

Regulatory Authorizations

United States Pending data

FDA UDI

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Manufacturer

Manufacturer
Responsive Orthopedics Llc

Sources (1)

  • FDA UDI deac9a53-494d-418c-b37b-f3d9bce196b0 34 fields · synced May 31, 2026