510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K934390Substantially Equivalent

Oscillating Bone Saw Blade, 6200 Series

Boehringer Laboratories, LLC, Norristown PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K934390 is the FDA 510(k) clearance record for OSCILLATING BONE SAW BLADE, 6200 SERIES, a class I device, cleared for Boehringer Laboratories on under FDA product code GFA (Blade, Saw, General & Plastic Surgery, Surgical). FDA records list 44 510(k) clearances for Boehringer Laboratories, from to . As of , FDA records show no recalls naming K934390.

Clearance record

Decision date
Received
(139 days to decision)
Product code
GFA Blade, Saw, General & Plastic Surgery, Surgical
Regulation
21 CFR 878.4820
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Boehringer Laboratories P.O. Box 870, Norristown PA
510(k) summary
Summary
Third party review
No

Clearances, product code GFA

Trailing 12 months

FDA records hold no clearances under product code GFA in the trailing twelve months.

FDA records show no clearances under product code GFA in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GFA, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260