ARTHROSCOPIC ANKLE HOLDER
K-Number: K864881 · 1986-12-29
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Device Summary
Frequently Asked Questions
What is the ARTHROSCOPIC ANKLE HOLDER?
ARTHROSCOPIC ANKLE HOLDER is a medical device that received FDA 510(k) clearance on 1986-12-29. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K864881.
When did ARTHROSCOPIC ANKLE HOLDER receive FDA 510(k) clearance?
ARTHROSCOPIC ANKLE HOLDER received FDA 510(k) clearance on 1986-12-29, under 510(k) number K864881.
Who is the listed applicant for ARTHROSCOPIC ANKLE HOLDER?
The FDA 510(k) record lists Orthopedic Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ARTHROSCOPIC ANKLE HOLDER?
The FDA product code for ARTHROSCOPIC ANKLE HOLDER 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 Orthopedic Systems, Inc. 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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