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FDA 510(k)

PRITCHARD SURFACE REPLACEMENT ELBOW

K-Number: K810847 · 1981-05-01

ApplicantDepuy, Inc.
Decision Date1981-05-01
Product CodeJDB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

PRITCHARD SURFACE REPLACEMENT ELBOW is the device name listed in this FDA 510(k) record. The listed applicant is Depuy, Inc.. It received FDA 510(k) clearance on 1981-05-01 under 510(k) number K810847. The device is classified under product code JDB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PRITCHARD SURFACE REPLACEMENT ELBOW?

PRITCHARD SURFACE REPLACEMENT ELBOW is a medical device that received FDA 510(k) clearance on 1981-05-01. The listed applicant is Depuy, Inc.. The 510(k) number is K810847.

When did PRITCHARD SURFACE REPLACEMENT ELBOW receive FDA 510(k) clearance?

PRITCHARD SURFACE REPLACEMENT ELBOW received FDA 510(k) clearance on 1981-05-01, under 510(k) number K810847.

Who is the listed applicant for PRITCHARD SURFACE REPLACEMENT ELBOW?

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

What is the FDA product code for PRITCHARD SURFACE REPLACEMENT ELBOW?

The FDA product code for PRITCHARD SURFACE REPLACEMENT ELBOW is JDB.

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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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