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

TABLE, HAND SURGI

K Number: K760456 · Decision Nov 2, 1976
Classifications
1
FEI Numbers
162
Registration Numbers
162
Same Product Code
60
Applicant Total
124
Review Days
77

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
TABLE, HAND SURGI
K Number
K760456
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
878.4950
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Applicant
Stryker Corp.
Date Received
August 17, 1976
Decision Date
November 2, 1976
Product Code
FWZ
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
FWZ Operating Room Accessories Table Tray

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (FWZ), 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. →