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FDA 510(k)

SIIS#1 TISSUE SUSPENSION SYSTEM

K-Number: K020705 · 2002-04-26

Decision Date2002-04-26
Product CodeOTN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SIIS#1 TISSUE SUSPENSION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Tag Medical Products. It received FDA 510(k) clearance on 2002-04-26 under 510(k) number K020705. The device is classified under product code OTN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIIS#1 TISSUE SUSPENSION SYSTEM?

SIIS#1 TISSUE SUSPENSION SYSTEM is a medical device that received FDA 510(k) clearance on 2002-04-26. The listed applicant is Tag Medical Products. The 510(k) number is K020705.

When did SIIS#1 TISSUE SUSPENSION SYSTEM receive FDA 510(k) clearance?

SIIS#1 TISSUE SUSPENSION SYSTEM received FDA 510(k) clearance on 2002-04-26, under 510(k) number K020705.

Who is the listed applicant for SIIS#1 TISSUE SUSPENSION SYSTEM?

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

What is the FDA product code for SIIS#1 TISSUE SUSPENSION SYSTEM?

The FDA product code for SIIS#1 TISSUE SUSPENSION SYSTEM is OTN.

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 Tag Medical Products 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.

Related Devices (Code: OTN)

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.

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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