OSTEO BOS SYSTEM IN STAINLESS STEEL
K-Number: K973204 · 1997-09-25
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Device Summary
Frequently Asked Questions
What is the OSTEO BOS SYSTEM IN STAINLESS STEEL?
OSTEO BOS SYSTEM IN STAINLESS STEEL is a medical device that received FDA 510(k) clearance on 1997-09-25. The listed applicant is Osteonics Corp.. The 510(k) number is K973204.
When did OSTEO BOS SYSTEM IN STAINLESS STEEL receive FDA 510(k) clearance?
OSTEO BOS SYSTEM IN STAINLESS STEEL received FDA 510(k) clearance on 1997-09-25, under 510(k) number K973204.
Who is the listed applicant for OSTEO BOS SYSTEM IN STAINLESS STEEL?
The FDA 510(k) record lists Osteonics Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OSTEO BOS SYSTEM IN STAINLESS STEEL?
The FDA product code for OSTEO BOS SYSTEM IN STAINLESS STEEL is HRS.
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 Osteonics Corp. 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: HRS)
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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