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CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER

K901677 Class I Traditional
Decision Date
1990-04-23
Sponsor / Applicant
Buckman Co., Inc.

Technical Specification

510(k) Submission ID K901677
Product Code LGH
Medical Specialty / Panel Orthopedic
Regulation Citation 21 CFR 888.5960
Decision Date 1990-04-23
Clearance Pathway Traditional

Official Documentation

FDA CDRH Summary / statement of record

View FDA Summary PDF

Clearance Summary

CARAPACE PORTABLE CAST SAW, SWISS-EX CAST CUTTER received FDA 510(k) clearance under submission number K901677, sponsored by Buckman Co., 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 1990-04-23.

Classification & Regulation

This clearance is catalogued under FDA product code LGH and 21 CFR 888.5960, within the Orthopedic review panel as a Class I device.