LRTM SURGICAL MESH
K-Number: K070560 · 2007-06-11
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Device Summary
Frequently Asked Questions
What is the LRTM SURGICAL MESH?
LRTM SURGICAL MESH is a medical device that received FDA 510(k) clearance on 2007-06-11. The listed applicant is Lifecell Corp.. The 510(k) number is K070560.
When did LRTM SURGICAL MESH receive FDA 510(k) clearance?
LRTM SURGICAL MESH received FDA 510(k) clearance on 2007-06-11, under 510(k) number K070560.
Who is the listed applicant for LRTM 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 LRTM SURGICAL MESH?
The FDA product code for LRTM 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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