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FDA 510(k)

OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM

K-Number: K954023 · 1995-11-22

Decision Date1995-11-22
Product CodeMEH
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Osteonics Corp.. It received FDA 510(k) clearance on 1995-11-22 under 510(k) number K954023. The device is classified under product code MEH. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM?

OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM is a medical device that received FDA 510(k) clearance on 1995-11-22. The listed applicant is Osteonics Corp.. The 510(k) number is K954023.

When did OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM receive FDA 510(k) clearance?

OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM received FDA 510(k) clearance on 1995-11-22, under 510(k) number K954023.

Who is the listed applicant for OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM?

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

What is the FDA product code for OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM?

The FDA product code for OSTEONICS SECUR-FIT HA PSL EXTRA ACETABULAR COMPONENT SYSTEM is MEH.

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 Osteonics Corp. 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 178 devices →

Related Devices (Code: MEH)

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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