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FDA 510(k)

Stryker Arthroscope

K-Number: K202659 · 2020-12-01

ApplicantStryker
Decision Date2020-12-01
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

Stryker Arthroscope is the device name listed in this FDA 510(k) record. The listed applicant is Stryker. It received FDA 510(k) clearance on 2020-12-01 under 510(k) number K202659. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Stryker Arthroscope?

Stryker Arthroscope is a medical device that received FDA 510(k) clearance on 2020-12-01. The listed applicant is Stryker. The 510(k) number is K202659.

When did Stryker Arthroscope receive FDA 510(k) clearance?

Stryker Arthroscope received FDA 510(k) clearance on 2020-12-01, under 510(k) number K202659.

Who is the listed applicant for Stryker Arthroscope?

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

What is the FDA product code for Stryker Arthroscope?

The FDA product code for Stryker Arthroscope is HRX.

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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.

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