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

TITAN RC TACK

K Number: K994269 · Decision Jan 10, 2000
Classifications
1
FEI Numbers
147
Registration Numbers
147
Same Product Code
219
Applicant Total
34
Review Days
21

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Basic Information

Device Name
TITAN RC TACK
K Number
K994269
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Innovasive Devices, Inc.
Date Received
December 20, 1999
Decision Date
January 10, 2000
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
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
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. →