FDA 510(k)

STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM

K-Number: K991703 · 1999-05-27

Decision Date1999-05-27

Product CodeGCJ

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Instruments. It received FDA 510(k) clearance on 1999-05-27 under 510(k) number K991703. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM?

STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM is a medical device that received FDA 510(k) clearance on 1999-05-27. The listed applicant is Stryker Instruments. The 510(k) number is K991703.

When did STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM receive FDA 510(k) clearance?

STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM received FDA 510(k) clearance on 1999-05-27, under 510(k) number K991703.

Who is the listed applicant for STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM?

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

What is the FDA product code for STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM?

The FDA product code for STRYKER HERMES-READY TOTAL PERFORMANCE SYSTEM is GCJ.

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Official Source

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