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FDA 510(k)

INTERLOCKING INTRAMEDULLARY NAILS

K-Number: K884610 · 1988-12-01

ApplicantDepuy, Inc.
Decision Date1988-12-01
Product CodeHSB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

INTERLOCKING INTRAMEDULLARY NAILS is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1988-12-01 under 510(k) number K884610. 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 INTERLOCKING INTRAMEDULLARY NAILS?

INTERLOCKING INTRAMEDULLARY NAILS is a medical device that received FDA 510(k) clearance on 1988-12-01. The listed applicant is Depuy, Inc.. The 510(k) number is K884610.

When did INTERLOCKING INTRAMEDULLARY NAILS receive FDA 510(k) clearance?

INTERLOCKING INTRAMEDULLARY NAILS received FDA 510(k) clearance on 1988-12-01, under 510(k) number K884610.

Who is the listed applicant for INTERLOCKING INTRAMEDULLARY NAILS?

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 INTERLOCKING INTRAMEDULLARY NAILS?

The FDA product code for INTERLOCKING INTRAMEDULLARY NAILS 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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