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FDA 510(k)

ASCENSION METAL GREAT TOE SYSTEM

K-Number: K092047 · 2010-01-14

Decision Date2010-01-14
Product CodeKWD
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ASCENSION METAL GREAT TOE SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Ascension Orthopedics, Inc.. It received FDA 510(k) clearance on 2010-01-14 under 510(k) number K092047. The device is classified under product code KWD. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASCENSION METAL GREAT TOE SYSTEM?

ASCENSION METAL GREAT TOE SYSTEM is a medical device that received FDA 510(k) clearance on 2010-01-14. The listed applicant is Ascension Orthopedics, Inc.. The 510(k) number is K092047.

When did ASCENSION METAL GREAT TOE SYSTEM receive FDA 510(k) clearance?

ASCENSION METAL GREAT TOE SYSTEM received FDA 510(k) clearance on 2010-01-14, under 510(k) number K092047.

Who is the listed applicant for ASCENSION METAL GREAT TOE SYSTEM?

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

What is the FDA product code for ASCENSION METAL GREAT TOE SYSTEM?

The FDA product code for ASCENSION METAL GREAT TOE SYSTEM is KWD.

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 Ascension Orthopedics, 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.

View all 22 devices →

Related Devices (Code: KWD)

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

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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