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FDA 510(k)

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS

K-Number: K974757 · 1998-03-05

ApplicantAcromed Corp.
Decision Date1998-03-05
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS is the device name listed in this FDA 510(k) record. The listed applicant is Acromed Corp.. It received FDA 510(k) clearance on 1998-03-05 under 510(k) number K974757. The device is classified under product code KWQ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS?

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS is a medical device that received FDA 510(k) clearance on 1998-03-05. The listed applicant is Acromed Corp.. The 510(k) number is K974757.

When did KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS receive FDA 510(k) clearance?

KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS received FDA 510(k) clearance on 1998-03-05, under 510(k) number K974757.

Who is the listed applicant for KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS?

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 KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS?

The FDA product code for KANEDA ANTERIOR SCOLIOSIS SYSTEM KASS 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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