Stryker Arthroscope
K-Number: K202659 · 2020-12-01
ApplicantStryker
Decision Date2020-12-01
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent
Device Summary
Stryker Arthroscope is a medical device manufactured by Stryker. It received FDA 510(k) clearance on 2020-12-01 under approval 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. It is manufactured by Stryker. The 510(k) number is K202659.
When was Stryker Arthroscope approved by the FDA?
Stryker Arthroscope received FDA 510(k) clearance on 2020-12-01, under approval number K202659.
What company makes Stryker Arthroscope?
Stryker Arthroscope is manufactured by Stryker.
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.