LTM-BPS SURGICAL MESH
K-Number: K082176 · 2008-11-14
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Device Summary
Frequently Asked Questions
What is the LTM-BPS SURGICAL MESH?
LTM-BPS SURGICAL MESH is a medical device that received FDA 510(k) clearance on 2008-11-14. The listed applicant is Lifecell Corp.. The 510(k) number is K082176.
When did LTM-BPS SURGICAL MESH receive FDA 510(k) clearance?
LTM-BPS SURGICAL MESH received FDA 510(k) clearance on 2008-11-14, under 510(k) number K082176.
Who is the listed applicant for LTM-BPS SURGICAL MESH?
The FDA 510(k) record lists Lifecell Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LTM-BPS SURGICAL MESH?
The FDA product code for LTM-BPS SURGICAL MESH is FTM.
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 Lifecell 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: FTM)
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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