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FDA 510(k)

MODIFIED TROCHANTER CABLE GRIP SYSTEM

K-Number: K872224 · 1987-08-17

Decision Date1987-08-17
Product CodeKTT
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MODIFIED TROCHANTER CABLE GRIP SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1987-08-17 under 510(k) number K872224. The device is classified under product code KTT. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED TROCHANTER CABLE GRIP SYSTEM?

MODIFIED TROCHANTER CABLE GRIP SYSTEM is a medical device that received FDA 510(k) clearance on 1987-08-17. The listed applicant is Howmedica Corp.. The 510(k) number is K872224.

When did MODIFIED TROCHANTER CABLE GRIP SYSTEM receive FDA 510(k) clearance?

MODIFIED TROCHANTER CABLE GRIP SYSTEM received FDA 510(k) clearance on 1987-08-17, under 510(k) number K872224.

Who is the listed applicant for MODIFIED TROCHANTER CABLE GRIP SYSTEM?

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 MODIFIED TROCHANTER CABLE GRIP SYSTEM?

The FDA product code for MODIFIED TROCHANTER CABLE GRIP SYSTEM is KTT.

Related Clinical Trials

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.

Other records listing Howmedica Corp. as applicant

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.

View all 373 devices →

Related Devices (Code: KTT)

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.

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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