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FDA 510(k)

ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION

K-Number: K873826 · 1988-11-30

ApplicantAcromed Corp.
Decision Date1988-11-30
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION is the device name listed in this FDA 510(k) record. The listed applicant is Acromed Corp.. It received FDA 510(k) clearance on 1988-11-30 under 510(k) number K873826. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION?

ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION is a medical device that received FDA 510(k) clearance on 1988-11-30. The listed applicant is Acromed Corp.. The 510(k) number is K873826.

When did ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION receive FDA 510(k) clearance?

ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION received FDA 510(k) clearance on 1988-11-30, under 510(k) number K873826.

Who is the listed applicant for ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION?

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

What is the FDA product code for ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION?

The FDA product code for ACROMED/KANEDA ANTERIOR SPINAL INSTRUMENTATION is KWQ.

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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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