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FDA 510(k)

EXETER X3 RIMFIT ACETABULAR CUP

K-Number: K111848 · 2011-10-05

ApplicantStryker Corp.
Decision Date2011-10-05
Product CodeJDI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

EXETER X3 RIMFIT ACETABULAR CUP is the device name listed in this FDA 510(k) record. The listed applicant is Stryker Corp.. It received FDA 510(k) clearance on 2011-10-05 under 510(k) number K111848. 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 EXETER X3 RIMFIT ACETABULAR CUP?

EXETER X3 RIMFIT ACETABULAR CUP is a medical device that received FDA 510(k) clearance on 2011-10-05. The listed applicant is Stryker Corp.. The 510(k) number is K111848.

When did EXETER X3 RIMFIT ACETABULAR CUP receive FDA 510(k) clearance?

EXETER X3 RIMFIT ACETABULAR CUP received FDA 510(k) clearance on 2011-10-05, under 510(k) number K111848.

Who is the listed applicant for EXETER X3 RIMFIT ACETABULAR CUP?

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

What is the FDA product code for EXETER X3 RIMFIT ACETABULAR CUP?

The FDA product code for EXETER X3 RIMFIT ACETABULAR CUP is JDI.

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Related Devices (Code: 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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