RecallHawk

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat

Kinetic Innovative Seating System, LLC

Summary

Kinetic Innovative Seating System, LLC received 510(k) clearance for KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat, a KNN device. Cleared on 2022-03-04.

Details

Source

510(k) Clearance

External ID

K211919

Action Date

2022-03-04

Status

Traditional

Category

device

Product Code

KNN

Product Description

KISS Dynamic Back Support, KISS Dynamic Solid Drop Seat. Product code: KNN.

Context & Analysis

A 510(k) clearance means the FDA determined this device is substantially equivalent to a legally marketed device. This is one of 403 device clearances issued this month.

Frequently Asked Questions

What does 510(k) clearance mean?

A 510(k) is an FDA premarket submission demonstrating that a device is substantially equivalent to a legally marketed device. It does NOT mean FDA approval — it means the device is cleared for marketing because it's similar enough to an existing cleared device. Most medical devices reach market via 510(k) rather than full PMA approval.

How often does Kinetic Innovative Seating System, LLC have FDA actions?

This is the only FDA action we have on record for Kinetic Innovative Seating System, LLC in our database.

Where can I find the official FDA record?

The official record is available on FDA.gov. Search for "K211919" on FDA.gov for the full record. You can also use the openFDA API to query this record programmatically.

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