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FDA 510(k)

WASHER, BOLT, NUT, ORTHOPEDIC

K-Number: K954682 · 1996-02-09

ApplicantLinvatec Corp.
Decision Date1996-02-09
Product CodeHTN
Advisory CommitteeOR
DecisionSubstantially Equivalent for Some Indications

Device Summary

WASHER, BOLT, NUT, ORTHOPEDIC is the device name listed in this FDA 510(k) record. The listed applicant is Linvatec Corp.. It received FDA 510(k) clearance on 1996-02-09 under 510(k) number K954682. The device is classified under product code HTN. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the WASHER, BOLT, NUT, ORTHOPEDIC?

WASHER, BOLT, NUT, ORTHOPEDIC is a medical device that received FDA 510(k) clearance on 1996-02-09. The listed applicant is Linvatec Corp.. The 510(k) number is K954682.

When did WASHER, BOLT, NUT, ORTHOPEDIC receive FDA 510(k) clearance?

WASHER, BOLT, NUT, ORTHOPEDIC received FDA 510(k) clearance on 1996-02-09, under 510(k) number K954682.

Who is the listed applicant for WASHER, BOLT, NUT, ORTHOPEDIC?

The FDA 510(k) record lists Linvatec Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for WASHER, BOLT, NUT, ORTHOPEDIC?

The FDA product code for WASHER, BOLT, NUT, ORTHOPEDIC is HTN.

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Related Devices (Code: HTN)

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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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