MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY
K-Number: K871804 · 1987-05-19
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Device Summary
Frequently Asked Questions
What is the MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY?
MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY is a medical device that received FDA 510(k) clearance on 1987-05-19. The listed applicant is Mcconnell Orthopedic. The 510(k) number is K871804.
When did MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY receive FDA 510(k) clearance?
MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY received FDA 510(k) clearance on 1987-05-19, under 510(k) number K871804.
Who is the listed applicant for MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY?
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 MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY?
The FDA product code for MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY 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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