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FDA 510(k)

LTM-BPS SURGICAL MESH

K-Number: K082176 · 2008-11-14

Decision Date2008-11-14
Product CodeFTM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

LTM-BPS SURGICAL MESH is the device name listed in this FDA 510(k) record. The listed applicant is Lifecell Corp.. It received FDA 510(k) clearance on 2008-11-14 under 510(k) number K082176. The device is classified under product code FTM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 10 devices →

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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