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OSTEONICS INSIGHT KNEE POSITIONING & ALIGNMENT SYSTEM

K953961 Class I Traditional
Decision Date
1995-11-29
Sponsor / Applicant
Osteonics Corp.

Technical Specification

510(k) Submission ID K953961
Product Code FWW
Medical Specialty / Panel General, Plastic Surgery
Regulation Citation 21 CFR 878.4960
Decision Date 1995-11-29
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

OSTEONICS INSIGHT KNEE POSITIONING & ALIGNMENT SYSTEM received FDA 510(k) clearance under submission number K953961, sponsored by Osteonics Corp.. 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 1995-11-29.

Classification & Regulation

This clearance is catalogued under FDA product code FWW and 21 CFR 878.4960, within the General, Plastic Surgery review panel as a Class I device.