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FDA 510(k)

RM ISOELASTIC BEVELLED ACETABULAR CUP

K-Number: K903116 · 1990-10-23

ApplicantRobert Mathys Co.
Decision Date1990-10-23
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

RM ISOELASTIC BEVELLED ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Robert Mathys Co.. It received FDA 510(k) clearance on 1990-10-23 under 510(k) number K903116. 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 RM ISOELASTIC BEVELLED ACETABULAR CUP?

RM ISOELASTIC BEVELLED ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 1990-10-23. The listed applicant is Robert Mathys Co.. The 510(k) number is K903116.

When did RM ISOELASTIC BEVELLED ACETABULAR CUP receive FDA 510(k) clearance?

RM ISOELASTIC BEVELLED ACETABULAR CUP received FDA 510(k) clearance on 1990-10-23, under 510(k) number K903116.

Who is the listed applicant for RM ISOELASTIC BEVELLED ACETABULAR CUP?

The FDA 510(k) record lists Robert Mathys Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for RM ISOELASTIC BEVELLED ACETABULAR CUP?

The FDA product code for RM ISOELASTIC BEVELLED ACETABULAR CUP is JDI.

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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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