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FDA 510(k)

ACROMED DOUBLE SUBLAMINAR WIRE

K-Number: K895413 · 1989-11-22

ApplicantAcromed Corp.
Decision Date1989-11-22
Product CodeKWP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACROMED DOUBLE SUBLAMINAR WIRE is the device name listed in this FDA 510(k) record. The listed applicant is Acromed Corp.. It received FDA 510(k) clearance on 1989-11-22 under 510(k) number K895413. The device is classified under product code KWP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACROMED DOUBLE SUBLAMINAR WIRE?

ACROMED DOUBLE SUBLAMINAR WIRE is a medical device that received FDA 510(k) clearance on 1989-11-22. The listed applicant is Acromed Corp.. The 510(k) number is K895413.

When did ACROMED DOUBLE SUBLAMINAR WIRE receive FDA 510(k) clearance?

ACROMED DOUBLE SUBLAMINAR WIRE received FDA 510(k) clearance on 1989-11-22, under 510(k) number K895413.

Who is the listed applicant for ACROMED DOUBLE SUBLAMINAR WIRE?

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 DOUBLE SUBLAMINAR WIRE?

The FDA product code for ACROMED DOUBLE SUBLAMINAR WIRE is KWP.

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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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