510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873690Substantially Equivalent

Cedar(tm) Pelvic Cushion

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

K873690 is the FDA 510(k) clearance record for CEDAR(TM) PELVIC CUSHION, a class I device, cleared for Cedar Surgical, Inc. on under FDA product code LWG (Surgical Table Cushion). FDA records list 17 510(k) clearances for Cedar Surgical, Inc., from to . As of , FDA records show no recalls naming K873690.

Clearance record

Decision date
Received
(48 days to decision)
Product code
LWG Surgical Table Cushion
Regulation
21 CFR 878.4950
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Cedar Surgical, Inc. 15265 Minnetonka Blvd., Minnetonka MN
Third party review
No

Clearances, product code LWG

Trailing 12 months

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

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