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

INNOVASIVE TIBIAL FASTENER

K Number: K983056 · Decision Oct 13, 1998
Classifications
1
FEI Numbers
275
Registration Numbers
275
Same Product Code
593
Applicant Total
34
Review Days
42

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
INNOVASIVE TIBIAL FASTENER
K Number
K983056
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3040
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innovasive Devices, Inc.
Date Received
September 1, 1998
Decision Date
October 13, 1998
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 Innovasive Devices, Inc.

K Number Device Name
K994269 TITAN RC TACK
K993975 ABSOLUTE ABSORBABLE INTERFERENCE SCREW
K992458 RC MULTISUTURE BONE ANCHOR, MODEL 4453/4454
K992377 RC TACK
K990454 BIO-INTERFERENCE SCREW
K984490 SUTURELESS ANCHOR
K983560 INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER
K981340 INNOVASIVE DEVICES MENISCAL DART REPAIR SYSTEM
K981193 INNOVASIVE 3.5MM METAL ROC XS SUTURE BONE FASTENER
K980491 INNOVASIVE LINX TIBIAL LIGAMENT FASTENER
Search all 34 clearances from Innovasive Devices, Inc. →