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SYNTHETIC SEEDING SPACER MODEL SS9 X 50-50, SS9 X 55-50, SS9 X 55-150, SS9 X 1CM-30

K100847 Class II Traditional
Decision Date
2010-05-21
Sponsor / Applicant
Biocompatibles, Inc.

Technical Specification

510(k) Submission ID K100847
Product Code KXK
Medical Specialty / Panel Radiology
Regulation Citation 21 CFR 892.5730
Decision Date 2010-05-21
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

SYNTHETIC SEEDING SPACER MODEL SS9 X 50-50, SS9 X 55-50, SS9 X 55-150, SS9 X 1CM-30 received FDA 510(k) clearance under submission number K100847, sponsored by Biocompatibles, Inc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Radiology review panel. The statutory decision date of record is 2010-05-21.

Classification & Regulation

This clearance is catalogued under FDA product code KXK and 21 CFR 892.5730, within the Radiology review panel as a Class II device.