510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K935357Substantially Equivalent

Snap Reciprocating Saw

Surgiquip, Inc., Tulsa OK / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K935357 is the FDA 510(k) clearance record for SNAP RECIPROCATING SAW, a class I device, cleared for Surgiquip, Inc. on under FDA product code GAF (Spatula, Surgical, General & Plastic Surgery). FDA records list 5 510(k) clearances for Surgiquip, Inc., from to . As of , FDA records show no recalls naming K935357.

Clearance record

Decision date
Received
(85 days to decision)
Product code
GAF Spatula, Surgical, General & Plastic Surgery
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Surgiquip, Inc. 1799 E. 71st St., Tulsa OK
510(k) summary
Summary
Third party review
No

Clearances, product code GAF

Trailing 12 months

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

FDA records show no clearances under product code GAF in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code GAF, 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