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

TECHMEDIA BONE STAPLE

K Number: K813567 · Decision Jan 12, 1982
Classifications
1
FEI Numbers
245
Registration Numbers
245
Same Product Code
230
Applicant Total
31
Review Days
21

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
TECHMEDIA BONE STAPLE
K Number
K813567
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
Techmedica, Inc.
Date Received
December 22, 1981
Decision Date
January 12, 1982
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 Techmedica, Inc.

K Number Device Name
K933935 CKS POROUS COATED FEMORAL COMPONENT
K932017 TECHMEDICA CONTINUUM HIP WITH HA COATING
K931929 TECHMEDICA CONTINUUM HIP SYSTEM
K926387 TECHMEDICA STANDARD CEMENTED HIP SYSTEM
K925420 TECHMEDICA STANDARD BIPOLAR SYSTEM
K923808 MULLER STRAIGHT STEM FEMORAL PROSTHESIS
K926579 TECHMEDICA 6.5MM SELF-TAPPING CANCELLOUS BONE SCRE
K911058 TECHMEDICA CAD/CAM CUSTOM HIP
K925181 TECHMEDICA MUELLER TYPE POLYETHYLENE ACETBUL CUP
K920080 CONTINUUM KNEE SYSTEM
Search all 31 clearances from Techmedica, Inc. →