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FDA 510(k)

LACTOSORB MENISCAL SCREW

K-Number: K002020 · 2000-08-25

ApplicantBiomet Manufacturing, Inc.
Decision Date2000-08-25
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LACTOSORB MENISCAL SCREW is the device name listed in this FDA 510(k) record. The listed applicant is Biomet Manufacturing, Inc.. It received FDA 510(k) clearance on 2000-08-25 under 510(k) number K002020. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACTOSORB MENISCAL SCREW?

LACTOSORB MENISCAL SCREW is a medical device that received FDA 510(k) clearance on 2000-08-25. The listed applicant is Biomet Manufacturing, Inc.. The 510(k) number is K002020.

When did LACTOSORB MENISCAL SCREW receive FDA 510(k) clearance?

LACTOSORB MENISCAL SCREW received FDA 510(k) clearance on 2000-08-25, under 510(k) number K002020.

Who is the listed applicant for LACTOSORB MENISCAL SCREW?

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

What is the FDA product code for LACTOSORB MENISCAL SCREW?

The FDA product code for LACTOSORB MENISCAL SCREW is MAI.

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Other records listing Biomet Manufacturing, Inc. 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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