OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM
K-Number: K962152 · 1996-08-14
Advertisement
Device Summary
Frequently Asked Questions
What is the OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM?
OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM is a medical device that received FDA 510(k) clearance on 1996-08-14. The listed applicant is Osteonics Corp.. The 510(k) number is K962152.
When did OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM receive FDA 510(k) clearance?
OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM received FDA 510(k) clearance on 1996-08-14, under 510(k) number K962152.
Who is the listed applicant for OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE 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 SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM?
The FDA product code for OSTEONICS SCORPIO POSTERIORLY STABILIZED TOTAL KNEE SYSTEM is JWH.
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: JWH)
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.
Advertisement