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

SLEEVE AND BUTTON SOFT TISSUE DEVICES

K Number: K071704 · Decision Sep 17, 2007
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
4
Review Days
88

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
SLEEVE AND BUTTON SOFT TISSUE DEVICES
K Number
K071704
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Biomet Sports Medicine, Inc.
Date Received
June 21, 2007
Decision Date
September 17, 2007
Product Code
MBI
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
MBI Fastener, Fixation, Nondegradable, Soft Tissue

Similar 510(k) Clearances

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

View all

Other Clearances by Biomet Sports Medicine, Inc.

K Number Device Name
K071816 HARPOON SUTURE ANCHOR
K070389 PEEK KNOTLESS ANCHORS
K071498 SUBTALAR IMPLANT