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FDA 510(k)

TRACER HIP PINNING SYSTEM

K-Number: K884406 · 1988-11-28

Decision Date1988-11-28
Product CodeJDS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

TRACER HIP PINNING SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is De Medica Mfg., Inc.. It received FDA 510(k) clearance on 1988-11-28 under 510(k) number K884406. The device is classified under product code JDS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRACER HIP PINNING SYSTEM?

TRACER HIP PINNING SYSTEM is a medical device that received FDA 510(k) clearance on 1988-11-28. The listed applicant is De Medica Mfg., Inc.. The 510(k) number is K884406.

When did TRACER HIP PINNING SYSTEM receive FDA 510(k) clearance?

TRACER HIP PINNING SYSTEM received FDA 510(k) clearance on 1988-11-28, under 510(k) number K884406.

Who is the listed applicant for TRACER HIP PINNING SYSTEM?

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

What is the FDA product code for TRACER HIP PINNING SYSTEM?

The FDA product code for TRACER HIP PINNING SYSTEM is JDS.

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 De Medica Mfg., Inc. 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.

Related Devices (Code: JDS)

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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