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FDA 510(k)

DURACON RECESSED PATELLA

K-Number: K951655 · 1995-07-11

ApplicantHowmedica Corp.
Decision Date1995-07-11
Product CodeJWH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

DURACON RECESSED PATELLA is the device name listed in this FDA 510(k) record. The listed applicant is Howmedica Corp.. It received FDA 510(k) clearance on 1995-07-11 under 510(k) number K951655. The device is classified under product code JWH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DURACON RECESSED PATELLA?

DURACON RECESSED PATELLA is a medical device that received FDA 510(k) clearance on 1995-07-11. The listed applicant is Howmedica Corp.. The 510(k) number is K951655.

When did DURACON RECESSED PATELLA receive FDA 510(k) clearance?

DURACON RECESSED PATELLA received FDA 510(k) clearance on 1995-07-11, under 510(k) number K951655.

Who is the listed applicant for DURACON RECESSED PATELLA?

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

What is the FDA product code for DURACON RECESSED PATELLA?

The FDA product code for DURACON RECESSED PATELLA is JWH.

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Other records listing Howmedica Corp. as applicant

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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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