Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MyKnee R Pin Positioners

K-Number: K220705 · 2022-05-04

Decision Date2022-05-04
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MyKnee R Pin Positioners is the device name listed in this FDA 510(k) record. The listed applicant is Medacta International S.A.. It received FDA 510(k) clearance on 2022-05-04 under 510(k) number K220705. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MyKnee R Pin Positioners?

MyKnee R Pin Positioners is a medical device that received FDA 510(k) clearance on 2022-05-04. The listed applicant is Medacta International S.A.. The 510(k) number is K220705.

When did MyKnee R Pin Positioners receive FDA 510(k) clearance?

MyKnee R Pin Positioners received FDA 510(k) clearance on 2022-05-04, under 510(k) number K220705.

Who is the listed applicant for MyKnee R Pin Positioners?

The FDA 510(k) record lists Medacta International S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MyKnee R Pin Positioners?

The FDA product code for MyKnee R Pin Positioners is JWH.

Other records listing Medacta International S.A. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

View all 146 devices →

Related Devices (Code: JWH)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.