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FDA 510(k)

ANTERIOR DYNAMIZED SYSTEM

K-Number: K953978 · 1997-02-19

ApplicantAcromed Corp.
Decision Date1997-02-19
Product CodeKWQ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ANTERIOR DYNAMIZED SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Acromed Corp.. It received FDA 510(k) clearance on 1997-02-19 under 510(k) number K953978. 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 ANTERIOR DYNAMIZED SYSTEM?

ANTERIOR DYNAMIZED SYSTEM is a medical device that received FDA 510(k) clearance on 1997-02-19. The listed applicant is Acromed Corp.. The 510(k) number is K953978.

When did ANTERIOR DYNAMIZED SYSTEM receive FDA 510(k) clearance?

ANTERIOR DYNAMIZED SYSTEM received FDA 510(k) clearance on 1997-02-19, under 510(k) number K953978.

Who is the listed applicant for ANTERIOR DYNAMIZED SYSTEM?

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 ANTERIOR DYNAMIZED SYSTEM?

The FDA product code for ANTERIOR DYNAMIZED SYSTEM 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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