ISLAND BIOSURGICAL BOLSTER
K-Number: K960101 · 1996-12-16
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Device Summary
Frequently Asked Questions
What is the ISLAND BIOSURGICAL BOLSTER?
ISLAND BIOSURGICAL BOLSTER is a medical device that received FDA 510(k) clearance on 1996-12-16. The listed applicant is Island Biosurgical, Inc.. The 510(k) number is K960101.
When did ISLAND BIOSURGICAL BOLSTER receive FDA 510(k) clearance?
ISLAND BIOSURGICAL BOLSTER received FDA 510(k) clearance on 1996-12-16, under 510(k) number K960101.
Who is the listed applicant for ISLAND BIOSURGICAL BOLSTER?
The FDA 510(k) record lists Island Biosurgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ISLAND BIOSURGICAL BOLSTER?
The FDA product code for ISLAND BIOSURGICAL BOLSTER is OTN.
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 Island Biosurgical, 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: OTN)
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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