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CUP BIOPSY FORCEPS, CURVED DOWN

K873505 Class I Traditional
Decision Date
1987-11-02
Sponsor / Applicant
Arthropedics, Inc.

Technical Specification

510(k) Submission ID K873505
Product Code HTD
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4800
Decision Date 1987-11-02
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CUP BIOPSY FORCEPS, CURVED DOWN received FDA 510(k) clearance under submission number K873505, sponsored by Arthropedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the General, Plastic Surgery review panel. The statutory decision date of record is 1987-11-02.

Classification & Regulation

This clearance is catalogued under FDA product code HTD and 21 CFR 878.4800, within the General, Plastic Surgery review panel as a Class I device.