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FDA 510(k)

HTO COMPRESSING STAPLE

K-Number: K895117 · 1990-05-09

ApplicantHowmedica Corp.
Decision Date1990-05-09
Product CodeJDR
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

HTO COMPRESSING STAPLE is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1990-05-09 under 510(k) number K895117. The device is classified under product code JDR. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HTO COMPRESSING STAPLE?

HTO COMPRESSING STAPLE is a medical device that received FDA 510(k) clearance on 1990-05-09. The listed applicant is Howmedica Corp.. The 510(k) number is K895117.

When did HTO COMPRESSING STAPLE receive FDA 510(k) clearance?

HTO COMPRESSING STAPLE received FDA 510(k) clearance on 1990-05-09, under 510(k) number K895117.

Who is the listed applicant for HTO COMPRESSING STAPLE?

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 HTO COMPRESSING STAPLE?

The FDA product code for HTO COMPRESSING STAPLE is JDR.

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Other records listing Howmedica Corp. as applicant

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Related Devices (Code: JDR)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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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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