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FDA 510(k)

STRYKER ARTHROSCOPE

K-Number: K093677 · 2010-03-05

ApplicantStryker Endoscopy
Decision Date2010-03-05
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 Endoscopy. It received FDA 510(k) clearance on 2010-03-05 under 510(k) number K093677. 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 2010-03-05. The listed applicant is Stryker Endoscopy. The 510(k) number is K093677.

When did STRYKER ARTHROSCOPE receive FDA 510(k) clearance?

STRYKER ARTHROSCOPE received FDA 510(k) clearance on 2010-03-05, under 510(k) number K093677.

Who is the listed applicant for STRYKER ARTHROSCOPE?

The FDA 510(k) record lists Stryker Endoscopy 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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Related Devices (Code: 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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