meddevicedb.com FDA Device Reference

ORTHOPEDIC PACKS

K951231 Class II Traditional
Decision Date
1995-12-01
Sponsor / Applicant
Sterile Concepts, Inc.

Technical Specification

510(k) Submission ID K951231
Product Code GAN
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4830
Decision Date 1995-12-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ORTHOPEDIC PACKS received FDA 510(k) clearance under submission number K951231, sponsored by Sterile Concepts, 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 1995-12-01.

Classification & Regulation

This clearance is catalogued under FDA product code GAN and 21 CFR 878.4830, within the General, Plastic Surgery review panel as a Class II device.