LATERAL BUTTRESS SUPPORT
K-Number: K905565 · 1991-02-21
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Device Summary
Frequently Asked Questions
What is the LATERAL BUTTRESS SUPPORT?
LATERAL BUTTRESS SUPPORT is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Mcconnell Orthopedic. The 510(k) number is K905565.
When did LATERAL BUTTRESS SUPPORT receive FDA 510(k) clearance?
LATERAL BUTTRESS SUPPORT received FDA 510(k) clearance on 1991-02-21, under 510(k) number K905565.
Who is the listed applicant for LATERAL BUTTRESS SUPPORT?
The FDA 510(k) record lists Mcconnell Orthopedic as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LATERAL BUTTRESS SUPPORT?
The FDA product code for LATERAL BUTTRESS SUPPORT is FWZ.
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 Mcconnell Orthopedic 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: FWZ)
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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