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METATARSAL DECOMPRESSION IMPLANT, MODEL 100

K090127 Class II Traditional
Decision Date
2009-05-01
Sponsor / Applicant
Solana Surgical, LLC

Technical Specification

510(k) Submission ID K090127
Product Code KWD
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.3730
Decision Date 2009-05-01
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

METATARSAL DECOMPRESSION IMPLANT, MODEL 100 received FDA 510(k) clearance under submission number K090127, sponsored by Solana Surgical, LLC. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 2009-05-01.

Classification & Regulation

This clearance is catalogued under FDA product code KWD and 21 CFR 888.3730, within the Orthopedic review panel as a Class II device.