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

BONE FIXATION NAIL

K Number: K943855 · Decision Jul 12, 1995
Classifications
1
FEI Numbers
115
Registration Numbers
115
Same Product Code
52
Applicant Total
43
Review Days
338

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
BONE FIXATION NAIL
K Number
K943855
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Acu Med, Inc.
Date Received
August 8, 1994
Decision Date
July 12, 1995
Product Code
JDS
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
JDS Nail, Fixation, Bone

Similar 510(k) Clearances

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

View all

Other Clearances by Acu Med, Inc.

K Number Device Name
K021321 WRIST FUSION PLATE
K013616 POLARUS CAP SCREW
K012655 CONGRUENT BONE PLATE SYSTEM
K992525 ACUMED MODULAR SHOULDER SYSTEM
K993657 ACUMED SUTURE ANCHOR
K980103 ACUMED SUTURE ANCHOR
K965028 ACUMED SUTURE WASHER
K965029 STABLELOC II EXTERNAL FIXATOR
K964500 ACUMED TENSION BAND PIN
K963026 TBD
Search all 43 clearances from Acu Med, Inc. →