MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE
K-Number: K862136 · 1986-07-14
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Device Summary
Frequently Asked Questions
What is the MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE?
MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE is a medical device that received FDA 510(k) clearance on 1986-07-14. The listed applicant is Dow Corning Wright. The 510(k) number is K862136.
When did MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE receive FDA 510(k) clearance?
MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE received FDA 510(k) clearance on 1986-07-14, under 510(k) number K862136.
Who is the listed applicant for MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE?
The FDA 510(k) record lists Dow Corning Wright as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE?
The FDA product code for MODIFIED WHITESIDE POSTERIOR STABILIZED TOTAL KNEE is HSX.
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 Dow Corning Wright 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: HSX)
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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