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FDA 510(k)

BONE NAIL, KUNTSCHER

K-Number: K911982 · 1991-07-26

ApplicantInternational Hospital Supply Co.
Decision Date1991-07-26
Product CodeHSD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BONE NAIL, KUNTSCHER is the device name listed in this FDA 510(k) record. The listed applicant is International Hospital Supply Co.. It received FDA 510(k) clearance on 1991-07-26 under 510(k) number K911982. The device is classified under product code HSD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BONE NAIL, KUNTSCHER?

BONE NAIL, KUNTSCHER is a medical device that received FDA 510(k) clearance on 1991-07-26. The listed applicant is International Hospital Supply Co.. The 510(k) number is K911982.

When did BONE NAIL, KUNTSCHER receive FDA 510(k) clearance?

BONE NAIL, KUNTSCHER received FDA 510(k) clearance on 1991-07-26, under 510(k) number K911982.

Who is the listed applicant for BONE NAIL, KUNTSCHER?

The FDA 510(k) record lists International Hospital Supply Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BONE NAIL, KUNTSCHER?

The FDA product code for BONE NAIL, KUNTSCHER is HSD.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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