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

LEIBINGER SELF-DRILLING SCREW

K Number: K970912 · Decision Oct 1, 1997
Classifications
1
FEI Numbers
659
Registration Numbers
659
Same Product Code
1058
Applicant Total
11
Review Days
203

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
LEIBINGER SELF-DRILLING SCREW
K Number
K970912
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Howmedica Leibinger, Inc.
Date Received
March 12, 1997
Decision Date
October 1, 1997
Product Code
HWC
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
HWC Screw, Fixation, Bone

Similar 510(k) Clearances

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

View all

Other Clearances by Howmedica Leibinger, Inc.

K Number Device Name
K972154 COHEN DISTRACTOR
K972166 GUERRERO - BELL DISTRACTOR
K961719 EPITEC TITANIUM IMPLANT SYSTEM FOR THE SURGICAL ANCHORING OF FACIAL PROSTHESES
K963030 LEIBINGER IMF SCREW
K970911 LEE PLATE
K963741 LEIBINGER LUHR SMALL CRANIOMAXILLOFACIAL BONE SCREWS
K964649 VAZQUEZ DINER INTRAORAL DISTRACTION DEVICE
K963739 LEIBINGER - LUHR SMALL ORTHOPEDIC BONE SCREWS
K963740 LEIBINGER - LUHR SMALL MANDIBULAR BONE SCREWS
K961120 MARKER SYSTEM FOR STEREOTAXIC NAVIGATION
Search all 11 clearances from Howmedica Leibinger, Inc. →