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FDA 510(k)

MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY

K-Number: K871804 · 1987-05-19

Decision Date1987-05-19
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MCCONNEL ORTHOPEDIC ARTHROSCOPY SUPPORT ASSEMBLY is the device name listed in this FDA 510(k) record. The listed applicant is Mcconnell Orthopedic. It received FDA 510(k) clearance on 1987-05-19 under 510(k) number K871804. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 16 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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