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FDA 510(k)

NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS

K-Number: K102806 · 2011-01-05

ApplicantAllergan Medical
Decision Date2011-01-05
Product CodeLCJ
DecisionSubstantially Equivalent

Device Summary

NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS is the device name listed in this FDA 510(k) record. The listed applicant is Allergan Medical. It received FDA 510(k) clearance on 2011-01-05 under 510(k) number K102806. The device is classified under product code LCJ. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS?

NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS is a medical device that received FDA 510(k) clearance on 2011-01-05. The listed applicant is Allergan Medical. The 510(k) number is K102806.

When did NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS receive FDA 510(k) clearance?

NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS received FDA 510(k) clearance on 2011-01-05, under 510(k) number K102806.

Who is the listed applicant for NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS?

The FDA 510(k) record lists Allergan Medical as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS?

The FDA product code for NATRELLE 133 TISSUE EXPANDER WITH SUTURE TABS is LCJ.

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Related Devices (Code: LCJ)

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.

K254126Natrelle 133S Tissue ExpandersAbbVieK242963MENTOR™ PliaForm™ Breast Tissue Expander w/ Suture TabsMentor Worldwide, LLCK243836Mentor™ CPX ™ 4 PLUS Enhance Breast Tissue ExpanderMentor Worldwide, LLCK241918MENTOR™ CPX™4 PLUS Enhance Breast Tissue ExpanderMentor Worldwide, LLCK211676Motiva Flora SmoothSilk Tissue ExpanderMotiva USA, LLCK214124AlloX2 Pro Tissue ExpandersSientra, Inc.

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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