MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL
K-Number: K952677 · 1995-08-21
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Device Summary
Frequently Asked Questions
What is the MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL?
MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL is a medical device that received FDA 510(k) clearance on 1995-08-21. The listed applicant is Porex Surgical, Inc.. The 510(k) number is K952677.
When did MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL receive FDA 510(k) clearance?
MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL received FDA 510(k) clearance on 1995-08-21, under 510(k) number K952677.
Who is the listed applicant for MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL?
The FDA 510(k) record lists Porex Surgical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL?
The FDA product code for MEDPOR BARRIER SURGICAL IMPLANT BIOMATERIAL is FWP.
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 Porex Surgical, 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: FWP)
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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