510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K090354Substantially Equivalent

Laminoplasty Plating System

Aesculap Implant System, Inc., Center Valley PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K090354 is the FDA 510(k) clearance record for LAMINOPLASTY PLATING SYSTEM, a class II device, cleared for Aesculap Implant System, Inc. on under FDA product code NQW (Orthosis, Spine, Plate, Laminoplasty, Metal). FDA's definition for product code NQW reads: "This device is a plate that is attached to the lamina after a laminoplasty or laminectomy procedure". FDA records list 18 510(k) clearances for Aesculap Implant System, Inc., from to . As of , FDA records show no recalls naming K090354.

Clearance record

Decision date
Received
(90 days to decision)
Product code
NQW Orthosis, Spine, Plate, Laminoplasty, Metal
Regulation
21 CFR 888.3050
Device class
Class II
Review panel
Orthopedic
Applicant
Aesculap Implant System, Inc. 3773 Corporate Pkwy., Center Valley PA
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NQW

Trailing 12 months
1 clearance under product code NQW in the twelve months to October 2026, May 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code NQW, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20261
June 20260
July 20260
August 20260
September 20260
October 20260