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FDA 510(k)

LACTOSORB MENISCAL REPAIR DEVICE

K-Number: K982095 · 1999-01-27

ApplicantBiomet, Inc.
Decision Date1999-01-27
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LACTOSORB MENISCAL REPAIR DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1999-01-27 under 510(k) number K982095. 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 REPAIR DEVICE?

LACTOSORB MENISCAL REPAIR DEVICE is a medical device that received FDA 510(k) clearance on 1999-01-27. The listed applicant is Biomet, Inc.. The 510(k) number is K982095.

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

LACTOSORB MENISCAL REPAIR DEVICE received FDA 510(k) clearance on 1999-01-27, under 510(k) number K982095.

Who is the listed applicant for LACTOSORB MENISCAL REPAIR DEVICE?

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 LACTOSORB MENISCAL REPAIR DEVICE?

The FDA product code for LACTOSORB MENISCAL REPAIR DEVICE is MAI.

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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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