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

SCISSOR, LEFT

K Number: K873501 · Decision Nov 2, 1987
Classifications
1
FEI Numbers
181
Registration Numbers
181
Same Product Code
7
Applicant Total
29
Review Days
63

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
SCISSOR, LEFT
K Number
K873501
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Arthropedics, Inc.
Date Received
August 31, 1987
Decision Date
November 2, 1987
Product Code
HRR
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

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

Product Code Device Name
HRR Scissors, Orthopedic, Surgical

Similar 510(k) Clearances

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

View all

Other Clearances by Arthropedics, Inc.

K Number Device Name
K873619 ARTHROSCOPIC RETENTION-MANIPULATION SYSTEM (ARMS)
K873655 MONOPOLAR CAUTERY RETROGADE TIP #TM-1703
K873653 MONOPOLAR CAUTERY BLADE TIP #TM-1701
K873654 MONOPOLAR CAUTERY CONICAL TIP #TM-1702
K873387 VIDEO ARTHROSCOPE, 1.7MM X 55 MM
K873504 CUP BIOPSY FORCEPS, RIGHT
K872533 THE CART
K873502 SCISSOR, RIGHT
K873512 SERRATED GRASPING FORCEPS, RIGHT
K873710 MAGNETIC RETRIEVER, 1.7MM W/LUER FITTING TM-1350
Search all 29 clearances from Arthropedics, Inc. →