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FDA 510(k)

ASCENSION SILLICONE MCP

K-Number: K022892 · 2002-11-25

Decision Date2002-11-25
Product CodeKYJ
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ASCENSION SILLICONE MCP 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 2002-11-25 under 510(k) number K022892. The device is classified under product code KYJ. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ASCENSION SILLICONE MCP?

ASCENSION SILLICONE MCP is a medical device that received FDA 510(k) clearance on 2002-11-25. The listed applicant is Ascension Orthopedics, Inc.. The 510(k) number is K022892.

When did ASCENSION SILLICONE MCP receive FDA 510(k) clearance?

ASCENSION SILLICONE MCP received FDA 510(k) clearance on 2002-11-25, under 510(k) number K022892.

Who is the listed applicant for ASCENSION SILLICONE MCP?

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 SILLICONE MCP?

The FDA product code for ASCENSION SILLICONE MCP is KYJ.

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: KYJ)

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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