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FDA 510(k)

COMMAND 2 MICOELECTRIC SURGICAL SYSTEM

K-Number: K961970 · 1996-07-26

ApplicantStryker Corp.
Decision Date1996-07-26
Product CodeHWE
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

COMMAND 2 MICOELECTRIC SURGICAL SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1996-07-26 under 510(k) number K961970. The device is classified under product code HWE. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COMMAND 2 MICOELECTRIC SURGICAL SYSTEM?

COMMAND 2 MICOELECTRIC SURGICAL SYSTEM is a medical device that received FDA 510(k) clearance on 1996-07-26. The listed applicant is Stryker Corp.. The 510(k) number is K961970.

When did COMMAND 2 MICOELECTRIC SURGICAL SYSTEM receive FDA 510(k) clearance?

COMMAND 2 MICOELECTRIC SURGICAL SYSTEM received FDA 510(k) clearance on 1996-07-26, under 510(k) number K961970.

Who is the listed applicant for COMMAND 2 MICOELECTRIC SURGICAL SYSTEM?

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

What is the FDA product code for COMMAND 2 MICOELECTRIC SURGICAL SYSTEM?

The FDA product code for COMMAND 2 MICOELECTRIC SURGICAL SYSTEM is HWE.

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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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