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FDA 510(k)

RIM-FIX, ACETABULAR CUP

K-Number: K993713 · 2000-01-28

ApplicantSurgical Implants, Inc.
Decision Date2000-01-28
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RIM-FIX, ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Implants, Inc.. It received FDA 510(k) clearance on 2000-01-28 under 510(k) number K993713. 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 RIM-FIX, ACETABULAR CUP?

RIM-FIX, ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 2000-01-28. The listed applicant is Surgical Implants, Inc.. The 510(k) number is K993713.

When did RIM-FIX, ACETABULAR CUP receive FDA 510(k) clearance?

RIM-FIX, ACETABULAR CUP received FDA 510(k) clearance on 2000-01-28, under 510(k) number K993713.

Who is the listed applicant for RIM-FIX, ACETABULAR CUP?

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

What is the FDA product code for RIM-FIX, ACETABULAR CUP?

The FDA product code for RIM-FIX, ACETABULAR CUP is JDI.

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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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