510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K930739Substantially Equivalent

Sutures Polyprop., Polyetheline, Nylon & Silk

Deknatel, Inc., San Jose-Heredia, CR / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K930739 is the FDA 510(k) clearance record for SUTURES POLYPROP., POLYETHELINE, NYLON & SILK, a class II device, cleared for Deknatel, Inc. on under FDA product code GAP (Suture, Nonabsorbable, Silk). FDA records list 37 510(k) clearances for Deknatel, Inc., from to . As of , FDA records show one recall naming K930739.

Clearance record

Decision date
Received
(529 days to decision)
Product code
GAP Suture, Nonabsorbable, Silk
Regulation
21 CFR 878.5030
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Deknatel, Inc. Kilometer 9 Carretera, San Jose-Heredia, CR
510(k) summary
Summary
Third party review
No

Clearances, product code GAP

Trailing 12 months

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

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