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FDA 510(k)

THARIES FIBER

K-Number: K855148 · 1986-02-18

ApplicantZimmer, Inc.
Decision Date1986-02-18
Product Code
DecisionSubstantially Equivalent for Some Indications

Device Summary

THARIES FIBER is the device name listed in this FDA 510(k) record. The listed applicant is Zimmer, Inc.. It received FDA 510(k) clearance on 1986-02-18 under 510(k) number K855148. FDA Decision: Substantially Equivalent for Some Indications.

Frequently Asked Questions

What is the THARIES FIBER?

THARIES FIBER is a medical device that received FDA 510(k) clearance on 1986-02-18. The listed applicant is Zimmer, Inc.. The 510(k) number is K855148.

When did THARIES FIBER receive FDA 510(k) clearance?

THARIES FIBER received FDA 510(k) clearance on 1986-02-18, under 510(k) number K855148.

Who is the listed applicant for THARIES FIBER?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

Other records listing Zimmer, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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