MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT
K-Number: K871821 · 1987-05-26
Advertisement
Device Summary
Frequently Asked Questions
What is the MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT?
MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT is a medical device that received FDA 510(k) clearance on 1987-05-26. The listed applicant is Mcconnell Orthopedic. The 510(k) number is K871821.
When did MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT receive FDA 510(k) clearance?
MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT received FDA 510(k) clearance on 1987-05-26, under 510(k) number K871821.
Who is the listed applicant for MCCONNELL ORTHOPEDIC POSTERIOR BODY 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 MCCONNELL ORTHOPEDIC POSTERIOR BODY SUPPORT?
The FDA product code for MCCONNELL ORTHOPEDIC POSTERIOR BODY 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.
Advertisement