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FDA 510(k)

NISONSON WIRE & DRILL GUIDE SYS

K-Number: K843348 · 1984-10-31

ApplicantStryker Corp.
Decision Date1984-10-31
Product Code
DecisionSubstantially Equivalent

Device Summary

NISONSON WIRE & DRILL GUIDE SYS is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 1984-10-31 under 510(k) number K843348. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NISONSON WIRE & DRILL GUIDE SYS?

NISONSON WIRE & DRILL GUIDE SYS is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is Stryker Corp.. The 510(k) number is K843348.

When did NISONSON WIRE & DRILL GUIDE SYS receive FDA 510(k) clearance?

NISONSON WIRE & DRILL GUIDE SYS received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843348.

Who is the listed applicant for NISONSON WIRE & DRILL GUIDE SYS?

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

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Other records listing Stryker Corp. as applicant

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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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