COLLINS POSITIONING DEVICE
K-Number: K864880 · 1986-12-29
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Device Summary
Frequently Asked Questions
What is the COLLINS POSITIONING DEVICE?
COLLINS POSITIONING DEVICE 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 K864880.
When did COLLINS POSITIONING DEVICE receive FDA 510(k) clearance?
COLLINS POSITIONING DEVICE received FDA 510(k) clearance on 1986-12-29, under 510(k) number K864880.
Who is the listed applicant for COLLINS POSITIONING DEVICE?
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 COLLINS POSITIONING DEVICE?
The FDA product code for COLLINS POSITIONING DEVICE 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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