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FDA 510(k)

SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM

K-Number: K060522 · 2006-04-11

Decision Date2006-04-11
Product CodeMAI
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Scandius Biomedical, Inc.. It received FDA 510(k) clearance on 2006-04-11 under 510(k) number K060522. The device is classified under product code MAI. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM?

SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM is a medical device that received FDA 510(k) clearance on 2006-04-11. The listed applicant is Scandius Biomedical, Inc.. The 510(k) number is K060522.

When did SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM receive FDA 510(k) clearance?

SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM received FDA 510(k) clearance on 2006-04-11, under 510(k) number K060522.

Who is the listed applicant for SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM?

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

What is the FDA product code for SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM?

The FDA product code for SCANDIUS TRITIS ABSORBABLE TIBIAL RECONSTRUCTION SYSTEM is MAI.

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 Scandius Biomedical, 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.

Related Devices (Code: MAI)

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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