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ADHOC CLAW

K023963 Class II Traditional
Decision Date
2003-05-05
Sponsor / Applicant
Future Medical Systems, Inc.

Technical Specification

510(k) Submission ID K023963
Product Code MBI
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3040
Decision Date 2003-05-05
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

ADHOC CLAW received FDA 510(k) clearance under submission number K023963, sponsored by Future Medical Systems, 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 2003-05-05.

Classification & Regulation

This clearance is catalogued under FDA product code MBI and 21 CFR 888.3040, within the Orthopedic review panel as a Class II device.