OSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMER— 510(k) K870157

Name: FDA 510(k) clearance K870157
Creator: U.S. Food and Drug Administration
Published: 1987-02-24

Substantially Equivalent

Micro-Aire Surgical Instruments, Inc.

FDA 510(k) clearance K870157 for OSCILLATING SAW/ RECIPROCATING SAW/ DRILL-REAMER, Substantially Equivalent on 1987-02-24. Applicant: Micro-Aire Surgical Instruments, Inc.. Device class: 1.

Clearance details

Applicant: Micro-Aire Surgical Instruments, Inc.
Product code: Code KFK
Device class: Class 1
Regulation: 21 CFR 878.4820
Advisory panel: General, Plastic Surgery
Date received: 1987-01-13
Decision date: 1987-02-24
Decision: Substantially Equivalent
Clearance type: Traditional
Location: San Fernando, CA, US

Download summary PDF View on FDA.gov ↗

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K893949 — #157 EXAM LIGHT1989-08-07
K894301 — MICRO-AIRE STERNUM SAW 48001989-08-03
K801737 — STERNUM SAW1980-08-20

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K903713 — OSTEOTOME MODEL NUMBERS 2500-228 & 2500-2291990-09-14
K903664 — MICRO-AIRE WIRE PASS AND CRANIOTOME DRILL1990-09-13

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