510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K161259Substantially Equivalent

KLS Martin Cannulated Headless Screws

KLS-Martin L.P., Jacksonville FL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K161259 is the FDA 510(k) clearance record for KLS Martin Cannulated Headless Screws, a class II device, cleared for KLS Martin L.P. on under FDA product code HWC (Screw, Fixation, Bone). FDA records list 78 510(k) clearances for KLS Martin L.P., from to . As of , FDA records show no recalls naming K161259.

Clearance record

Decision date
Received
(229 days to decision)
Product code
HWC Screw, Fixation, Bone
Regulation
21 CFR 888.3040
Device class
Class II
Review panel
Orthopedic
Applicant
KLS Martin L.P. 11201 Saint Johns Industrial Pkwy. S, Jacksonville FL
510(k) summary
Summary PDF
Third party review
No

Clearances, product code HWC

Trailing 12 months
21 clearances under product code HWC in the twelve months to October 2026, May 2026 the highest month at 4.
Show the numbers
Monthly 510(k) clearances under FDA product code HWC, trailing twelve months
MonthClearances
November 20251
December 20251
January 20260
February 20260
March 20262
April 20263
May 20264
June 20262
July 20261
August 20263
September 20264
October 20260