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FDA 510(k)

IM C-MENT ACETABULAR CAP

K-Number: K955137 · 1996-10-10

Decision Date1996-10-10
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

IM C-MENT ACETABULAR CAP is the device name listed in this FDA 510(k) record. The listed applicant is Implant Ideas, LLC. It received FDA 510(k) clearance on 1996-10-10 under 510(k) number K955137. The device is classified under product code JDI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IM C-MENT ACETABULAR CAP?

IM C-MENT ACETABULAR CAP is a medical device that received FDA 510(k) clearance on 1996-10-10. The listed applicant is Implant Ideas, LLC. The 510(k) number is K955137.

When did IM C-MENT ACETABULAR CAP receive FDA 510(k) clearance?

IM C-MENT ACETABULAR CAP received FDA 510(k) clearance on 1996-10-10, under 510(k) number K955137.

Who is the listed applicant for IM C-MENT ACETABULAR CAP?

The FDA 510(k) record lists Implant Ideas, LLC as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IM C-MENT ACETABULAR CAP?

The FDA product code for IM C-MENT ACETABULAR CAP is JDI.

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.

Related Devices (Code: JDI)

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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