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CALMPS: BONE, MASTIN, LEWIN, BRAND

K930028 Class I Traditional
Decision Date
1993-02-16
Sponsor / Applicant
Thomasville Medical Assoc.

Technical Specification

510(k) Submission ID K930028
Product Code LXH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.4540
Decision Date 1993-02-16
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CALMPS: BONE, MASTIN, LEWIN, BRAND received FDA 510(k) clearance under submission number K930028, sponsored by Thomasville Medical Assoc.. The device was reviewed via the Traditional premarket notification pathway and assigned to the Orthopedic review panel. The statutory decision date of record is 1993-02-16.

Classification & Regulation

This clearance is catalogued under FDA product code LXH and 21 CFR 888.4540, within the Orthopedic review panel as a Class I device.