FDA 510(k)

EXETER HIP SYSTEM WITH V40 TAPER

K-Number: K011623 · 2001-06-15

Decision Date2001-06-15

Product CodeJDI

Advisory CommitteeOR

DecisionSubstantially Equivalent

Device Summary

EXETER HIP SYSTEM WITH V40 TAPER is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Osteonics Corp.. It received FDA 510(k) clearance on 2001-06-15 under 510(k) number K011623. 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 HIP SYSTEM WITH V40 TAPER?

EXETER HIP SYSTEM WITH V40 TAPER is a medical device that received FDA 510(k) clearance on 2001-06-15. The listed applicant is Howmedica Osteonics Corp.. The 510(k) number is K011623.

When did EXETER HIP SYSTEM WITH V40 TAPER receive FDA 510(k) clearance?

EXETER HIP SYSTEM WITH V40 TAPER received FDA 510(k) clearance on 2001-06-15, under 510(k) number K011623.

Who is the listed applicant for EXETER HIP SYSTEM WITH V40 TAPER?

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

What is the FDA product code for EXETER HIP SYSTEM WITH V40 TAPER?

The FDA product code for EXETER HIP SYSTEM WITH V40 TAPER 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.