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FDA 510(k)

LACTOSORB PANELS AND FASTENERS

K-Number: K980927 · 1998-06-05

ApplicantBiomet, Inc.
Decision Date1998-06-05
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

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 1998-06-05 under 510(k) number K980927. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LACTOSORB PANELS AND FASTENERS?

LACTOSORB PANELS AND FASTENERS is a medical device that received FDA 510(k) clearance on 1998-06-05. The listed applicant is Biomet, Inc.. The 510(k) number is K980927.

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

LACTOSORB PANELS AND FASTENERS received FDA 510(k) clearance on 1998-06-05, under 510(k) number K980927.

Who is the listed applicant for 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 LACTOSORB PANELS AND FASTENERS?

The FDA product code for LACTOSORB PANELS AND FASTENERS is JEY.

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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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