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FDA 510(k)

LACTOSORB BONE PIN

K-Number: K953194 · 1995-10-31

ApplicantBiomet, Inc.
Decision Date1995-10-31
Product CodeHTY
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

LACTOSORB BONE PIN is the device name listed in this FDA 510(k) record. The listed applicant is Biomet, Inc.. It received FDA 510(k) clearance on 1995-10-31 under 510(k) number K953194. The device is classified under product code HTY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the LACTOSORB BONE PIN?

LACTOSORB BONE PIN is a medical device that received FDA 510(k) clearance on 1995-10-31. The listed applicant is Biomet, Inc.. The 510(k) number is K953194.

When did LACTOSORB BONE PIN receive FDA 510(k) clearance?

LACTOSORB BONE PIN received FDA 510(k) clearance on 1995-10-31, under 510(k) number K953194.

Who is the listed applicant for LACTOSORB BONE PIN?

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 BONE PIN?

The FDA product code for LACTOSORB BONE PIN is HTY.

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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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