510(K) CLEARANCES 51 ▲2RECALLS POSTED 25 ▲2CLASS I 1PMA DECISIONS 50 ▲13WEEK ENDING / FDA DATA AS OF
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K981717Substantially Equivalent

Stryker Knifelight, Stryker Illuminated Retractor

Stryker Corp., Kalamazoo MI / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K981717 is the FDA 510(k) clearance record for STRYKER KNIFELIGHT, STRYKER ILLUMINATED RETRACTOR, a class II device, cleared for Stryker Instruments on under FDA product code FTD (Lamp, Surgical). FDA records list 568 510(k) clearances for STRYKER CORP., from to . As of , FDA records show no recalls naming K981717.

Clearance record

Decision date
Received
(46 days to decision)
Product code
FTD Lamp, Surgical
Regulation
21 CFR 878.4580
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Stryker Instruments 4100 E. Milham Ave., Kalamazoo MI
510(k) summary
Summary
Third party review
No

Clearances, product code FTD

Trailing 12 months

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

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