BONE CUTTING INSTRUMENTS & ACCESSORIES— 510(k) K874961

Name: FDA 510(k) clearance K874961
Creator: U.S. Food and Drug Administration
Published: 1987-12-30

Substantially Equivalent

Solway, Inc.

FDA 510(k) clearance K874961 for BONE CUTTING INSTRUMENTS & ACCESSORIES, Substantially Equivalent on 1987-12-30. Applicant: Solway, Inc.. Device class: 1.

Clearance details

Applicant: Solway, Inc.
Product code: Code GDR
Device class: Class 1
Regulation: 21 CFR 878.4800
Advisory panel: General, Plastic Surgery
Date received: 1987-12-02
Decision date: 1987-12-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Hollywood, FL, US

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K874956 — SELF-RETAINING RETRACTOR FOR NEUROSURGERY1988-01-28
K874964 — DENTAL HAND INSTRUMENTS1988-01-27
K875043 — RONGEUR (NEUROSURGICAL INSTRUMENTS)1988-01-22

Data sourced from openFDA. This site is unofficial and independent of the FDA.