OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION
K-Number: K880263 · 1988-03-15
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Device Summary
Frequently Asked Questions
What is the OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION?
OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION is a medical device that received FDA 510(k) clearance on 1988-03-15. The listed applicant is Orthopedic Systems, Inc.. The 510(k) number is K880263.
When did OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION receive FDA 510(k) clearance?
OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION received FDA 510(k) clearance on 1988-03-15, under 510(k) number K880263.
Who is the listed applicant for OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION?
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 OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION?
The FDA product code for OSI RIZZOLI ORTHOPEDIC TABLE/MANUAL VERSION is JEB.
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: JEB)
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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