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FDA 510(k)

ALLOCRAFT DBM

K-Number: K052735 · 2005-12-28

ApplicantLifecell Corp.
Decision Date2005-12-28
Product CodeMBP
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ALLOCRAFT DBM is the device name listed in this FDA 510(k) record. The listed applicant is Lifecell Corp.. It received FDA 510(k) clearance on 2005-12-28 under 510(k) number K052735. The device is classified under product code MBP. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLOCRAFT DBM?

ALLOCRAFT DBM is a medical device that received FDA 510(k) clearance on 2005-12-28. The listed applicant is Lifecell Corp.. The 510(k) number is K052735.

When did ALLOCRAFT DBM receive FDA 510(k) clearance?

ALLOCRAFT DBM received FDA 510(k) clearance on 2005-12-28, under 510(k) number K052735.

Who is the listed applicant for ALLOCRAFT DBM?

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 ALLOCRAFT DBM?

The FDA product code for ALLOCRAFT DBM is MBP.

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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.

K130817LTN - LAPAROSCOPIC SURGICAL MESHK112534LIFECELL TISSUE EXPANDERK121289LTM-LABAROSCOPIC SURGICAL MESHK082176LTM-BPS SURGICAL MESHK082103LTM WOUND DRESSINGK080353LTM-T SURGICAL MESH

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Related Devices (Code: MBP)

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.

K242799PliaFX FloLifenet HealthK130703VIVORTE BVFVivorte, Inc.K130498OSTEOSELECT DEMINERALIZED BONE MATRIX PUTTYBacterin International, Inc.K122513CLEARED UNDER GRAFTON II EDBMMedtronic Sofamor Danek, Inc.K113728SURFUSE GEL AND PUTTY, EXFUSE GEL AND PUTTYHans Biomed Corp.K103742ACCELL EVO3 (FORMERLY ACCELL A2I)Integra Life Sciences

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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