FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

FASCIA CUTTER

K Number: K834514 · Decision Mar 12, 1984
Classifications
1
FEI Numbers
300
Registration Numbers
300
Same Product Code
47
Applicant Total
124
Review Days
82

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
FASCIA CUTTER
K Number
K834514
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4800
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Stryker Corp.
Date Received
December 21, 1983
Decision Date
March 12, 1984
Product Code
GES
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GES Blade, Scalpel

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (GES), ordered by most recent decision date.

View all

Other Clearances by Stryker Corp.

K Number Device Name
K230045 HipCheck
K191259 Stryker CrossFlow Integrated Arthroscopy Pump
K182359 HipCheck
K143399 Stryker Footed Attachments and Cutting Accessories
K143320 Stryker Elite Attachments, Stryker Heavy Duty (HD) Attachments
K150449 LITe Plate System
K142381 Xia 3 Spinal System
K133671 ICONIX ALL SUTURE ANCHORS
K122113 MEMORY METAL STAPLES, EASYCLIP
K122284 HOFFMANN 3
Search all 124 clearances from Stryker Corp. →