Medical Device
Manufacturing
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K160493Substantially Equivalent

Cytosurg non-resorbable PTFE Membrane, 25mm x 30mm, Cytosurg non-resorbable PTFE Membrane, 12mm x 24mm

Salvin Dental Specialties, LLC, Charlotte NC / Traditional, Substantially Equivalent

K160493 is the FDA 510(k) clearance record for Cytosurg non-resorbable PTFE Membrane, 25mm x 30mm, Cytosurg non-resorbable PTFE Membrane, 12mm x 24mm, a class II device, cleared for Salvin Dental Specialties on under FDA product code NPK (Barrier, Synthetic, Intraoral). FDA's definition for product code NPK reads: "A synthetic dental barrier is a synthetic material device, such as ptfe, intended to aid in guided tissue and/or bone regeneration procedures and to act as a stable barrier for the containment of bone graft materials". FDA records list 4 510(k) clearances for Salvin Dental Specialties, from to . As of , FDA records show no recalls naming K160493.

Clearance record

Decision date
Received
(199 days to decision)
Product code
NPK Barrier, Synthetic, Intraoral
Regulation
21 CFR 872.3930
Device class
Class II
Review panel
Dental
Applicant
Salvin Dental Specialties 3450 Latrobe Dr., Charlotte NC
510(k) summary
Summary PDF
Third party review
No

Clearances, product code NPK

Trailing 12 months

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

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