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FDA 510(k)

BIOMET LATERAL TROCH PLATE

K-Number: K003294 · 2000-11-03

ApplicantBiomet, Inc.
Decision Date2000-11-03
Product CodeJDW
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

BIOMET LATERAL TROCH PLATE is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2000-11-03 under 510(k) number K003294. The device is classified under product code JDW. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOMET LATERAL TROCH PLATE?

BIOMET LATERAL TROCH PLATE is a medical device that received FDA 510(k) clearance on 2000-11-03. The listed applicant is Biomet, Inc.. The 510(k) number is K003294.

When did BIOMET LATERAL TROCH PLATE receive FDA 510(k) clearance?

BIOMET LATERAL TROCH PLATE received FDA 510(k) clearance on 2000-11-03, under 510(k) number K003294.

Who is the listed applicant for BIOMET LATERAL TROCH PLATE?

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

What is the FDA product code for BIOMET LATERAL TROCH PLATE?

The FDA product code for BIOMET LATERAL TROCH PLATE is JDW.

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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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