510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
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K982313Substantially Equivalent

Horizon Titanium Clips, Horizon Tantalum Clips

Weck Closure Systems, Research Triangle Park NC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K982313 is the FDA 510(k) clearance record for HORIZON TITANIUM CLIPS, HORIZON TANTALUM CLIPS, a class II device, cleared for Weck Closure Systems on under FDA product code FZP (Clip, Implantable). FDA records list 6 510(k) clearances for Weck Closure Systems, from to . As of , FDA records show one recall naming K982313.

Clearance record

Decision date
Received
(40 days to decision)
Product code
FZP Clip, Implantable
Regulation
21 CFR 878.4300
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Weck Closure Systems 1 Weck Dr., Research Triangle Park NC
510(k) summary
Statement
Third party review
No

Clearances, product code FZP

Trailing 12 months
5 clearances under product code FZP in the twelve months to October 2026, December 2025 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FZP, trailing twelve months
MonthClearances
November 20251
December 20252
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20261
August 20260
September 20261
October 20260