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

SUTURELESS ANCHOR

K Number: K984490 · Decision Mar 1, 1999
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
34
Review Days
74

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Basic Information

Device Name
SUTURELESS ANCHOR
K Number
K984490
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innovasive Devices, Inc.
Date Received
December 17, 1998
Decision Date
March 1, 1999
Product Code
MAI
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
MAI Fastener, Fixation, Biodegradable, Soft Tissue

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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
K983560 INNOVASIVE DEVICES INTRATUNNEL TIBIAL FIXATION FASTENER
K983056 INNOVASIVE TIBIAL 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. →