FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

STRYKER TOTAL PERFORMANCE SYSTEM

K Number: K943569 · Decision Jan 9, 1995
Classifications
1
FEI Numbers
131
Registration Numbers
131
Same Product Code
90
Applicant Total
124
Review Days
171

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
STRYKER TOTAL PERFORMANCE SYSTEM
K Number
K943569
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
874.4250
Medical Specialty
Ear, Nose, Throat
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Stryker Corp.
Date Received
July 22, 1994
Decision Date
January 9, 1995
Product Code
ERL
Advisory Committee
Ear, Nose, Throat
Review Advisory Committee
EN
Third Party
N

Classifications

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

Product Code Device Name
ERL Drill, Surgical, Ent (Electric Or Pneumatic) Including Handpiece

Similar 510(k) Clearances

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