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FDA 510(k)

HI MARC INTERLOCKING NAIL

K-Number: K871872 · 1987-06-23

ApplicantDepuy, Inc.
Decision Date1987-06-23
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HI MARC INTERLOCKING NAIL is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1987-06-23 under 510(k) number K871872. The device is classified under product code HSB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HI MARC INTERLOCKING NAIL?

HI MARC INTERLOCKING NAIL is a medical device that received FDA 510(k) clearance on 1987-06-23. The listed applicant is Depuy, Inc.. The 510(k) number is K871872.

When did HI MARC INTERLOCKING NAIL receive FDA 510(k) clearance?

HI MARC INTERLOCKING NAIL received FDA 510(k) clearance on 1987-06-23, under 510(k) number K871872.

Who is the listed applicant for HI MARC INTERLOCKING NAIL?

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

What is the FDA product code for HI MARC INTERLOCKING NAIL?

The FDA product code for HI MARC INTERLOCKING NAIL is HSB.

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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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