OSTEONICS RESTORATION HA HIP STEMS
K-Number: K983870 · 1998-12-02
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Device Summary
Frequently Asked Questions
What is the OSTEONICS RESTORATION HA HIP STEMS?
OSTEONICS RESTORATION HA HIP STEMS is a medical device that received FDA 510(k) clearance on 1998-12-02. The listed applicant is Osteonics Corp.. The 510(k) number is K983870.
When did OSTEONICS RESTORATION HA HIP STEMS receive FDA 510(k) clearance?
OSTEONICS RESTORATION HA HIP STEMS received FDA 510(k) clearance on 1998-12-02, under 510(k) number K983870.
Who is the listed applicant for OSTEONICS RESTORATION HA HIP STEMS?
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 RESTORATION HA HIP STEMS?
The FDA product code for OSTEONICS RESTORATION HA HIP STEMS 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.
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
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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