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FDA 510(k)

LORENZ LACTOSORB PANELS AND FASTENERS

K-Number: K011139 · 2001-12-20

ApplicantBiomet, Inc.
Decision Date2001-12-20
Product CodeHRS
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LORENZ LACTOSORB PANELS AND FASTENERS is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 2001-12-20 under 510(k) number K011139. The device is classified under product code HRS. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LORENZ LACTOSORB PANELS AND FASTENERS?

LORENZ LACTOSORB PANELS AND FASTENERS is a medical device that received FDA 510(k) clearance on 2001-12-20. The listed applicant is Biomet, Inc.. The 510(k) number is K011139.

When did LORENZ LACTOSORB PANELS AND FASTENERS receive FDA 510(k) clearance?

LORENZ LACTOSORB PANELS AND FASTENERS received FDA 510(k) clearance on 2001-12-20, under 510(k) number K011139.

Who is the listed applicant for LORENZ LACTOSORB PANELS AND FASTENERS?

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 LORENZ LACTOSORB PANELS AND FASTENERS?

The FDA product code for LORENZ LACTOSORB PANELS AND FASTENERS is HRS.

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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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