meddevicedb.com FDA Device Reference

ASCENSION PYROSPHERE (PCS)

K042690 Class II Traditional
Decision Date
2004-11-13
Sponsor / Applicant
Ascension Orthopedics, Inc.

Technical Specification

510(k) Submission ID K042690
Product Code KYI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3770
Decision Date 2004-11-13
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ASCENSION PYROSPHERE (PCS) received FDA 510(k) clearance under submission number K042690, sponsored by Ascension Orthopedics, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2004-11-13.

Classification & Regulation

This clearance is catalogued under FDA product code KYI and 21 CFR 888.3770, within the Orthopedic review panel as a Class II device.