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

DAY STAPLE

K Number: K853267 · Decision Sep 6, 1985
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
25
Review Days
32

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
DAY STAPLE
K Number
K853267
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent for Some Indications
Applicant
Protek, Inc.
Date Received
August 5, 1985
Decision Date
September 6, 1985
Product Code
JDR
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
JDR Staple, Fixation, Bone

Similar 510(k) Clearances

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

View all

Other Clearances by Protek, Inc.

K Number Device Name
K893785 ARC-2F ACETABULAR CUP
K893959 P.S.A. FEMORAL HIP PROSTHESIS
K892059 FEMORAL HEADS/MODULAR & FIXED W/ TITAN NITRIDE SUR
K883794 RESUBMITTED CLW ACETABULAR CUP W/SULMESH
K884952 VARIOUS FEMORAL HIP PROSTHESES W/SELF LOCK CERAMIC
K884889 MODIFIED O.E.C. UNIV. SELF-ALIGNING ACETA. COMP.
K884789 NEW JERSEY FEMORAL HIP PROSTHESIS FOR CEMENT APPLI
K890054 M.E.M. ACETABULAR CUP W/SULMESH FOR CEMENT APPLI.
K884888 MODIFIED NEW JERSEY ACETABULAR COMP. & BONE SCREWS
K882671 SAMUELSON SCREWLOC CUP
Search all 25 clearances from Protek, Inc. →