Cleared Traditional

SEARE BIOMEDICAL PECTORALIS IMPLANT

K982762 · Seare Biomedical Corp. · General & Plastic Surgery
Sep 1998
Decision
55d
Days
Class 2
Risk

About This 510(k) Submission

K982762 is an FDA 510(k) clearance for the SEARE BIOMEDICAL PECTORALIS IMPLANT, a Implant, Muscle, Pectoralis (Class II — Special Controls, product code MIC), submitted by Seare Biomedical Corp. (Salt Lake City, US). The FDA issued a Cleared decision on September 30, 1998, 55 days after receiving the submission on August 6, 1998. This device falls under the General & Plastic Surgery review panel. Regulated under 21 CFR 874.3620.

Submission Details

510(k) Number K982762 FDA.gov
FDA Decision Cleared SESE
Date Received August 06, 1998
Decision Date September 30, 1998
Days to Decision 55 days
Submission Type Traditional
Review Panel General & Plastic Surgery (SU)
Summary Summary PDF

Device Classification

Product Code MIC — Implant, Muscle, Pectoralis
Device Class Class II — Special Controls
CFR Regulation 21 CFR 874.3620

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