510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K863415Substantially Equivalent

Raylor Bone Impactors

Cedar Surgical, Inc., Minnetonka MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K863415 is the FDA 510(k) clearance record for RAYLOR BONE IMPACTORS, a class I device, cleared for Cedar Surgical, Inc. on under FDA product code HAO (Instrument, Surgical, Non-Powered). FDA records list 17 510(k) clearances for Cedar Surgical, Inc., from to . As of , FDA records show no recalls naming K863415.

Clearance record

Decision date
Received
(21 days to decision)
Product code
HAO Instrument, Surgical, Non-Powered
Regulation
21 CFR 882.4535
Device class
Class I
Review panel
Neurology
Applicant
Cedar Surgical, Inc. 15265 Minnetonka Blvd., Minnetonka MN
Third party review
No

Clearances, product code HAO

Trailing 12 months

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

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