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FDA 510(k)

NAIL, MASSIE II

K-Number: K780187 · 1978-03-15

ApplicantHowmedica Corp.
Decision Date1978-03-15
Product CodeJDO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

NAIL, MASSIE II is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1978-03-15 under 510(k) number K780187. The device is classified under product code JDO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NAIL, MASSIE II?

NAIL, MASSIE II is a medical device that received FDA 510(k) clearance on 1978-03-15. The listed applicant is Howmedica Corp.. The 510(k) number is K780187.

When did NAIL, MASSIE II receive FDA 510(k) clearance?

NAIL, MASSIE II received FDA 510(k) clearance on 1978-03-15, under 510(k) number K780187.

Who is the listed applicant for NAIL, MASSIE II?

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

What is the FDA product code for NAIL, MASSIE II?

The FDA product code for NAIL, MASSIE II is JDO.

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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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