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

LACTOSORB MENISCAL REPAIR DEVICE

K Number: K982095 · Decision Jan 27, 1999
Classifications
1
FEI Numbers
140
Registration Numbers
140
Same Product Code
213
Applicant Total
404
Review Days
226

Basic Information

Device Name
LACTOSORB MENISCAL REPAIR DEVICE
K Number
K982095
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
888.3030
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BIOMET, INC.
Date Received
June 15, 1998
Decision Date
January 27, 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

Similar 510(k) Clearances

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

View all

Other Clearances by BIOMET, INC.

K Number Device Name
K161592 Persona Partial Knee System
K161166 StageOne Select Cement Spacer Molds for Temporary Hip Replacement
K153657 Vanguard XP Knee System
K152621 OSS/Arcos IM Total Femur Rod
K150850 Refobacin Bone Cement R
K150867 Affixus Tibial Nailing System
K150522 G7 Dual Mobility System
K150503 Echo Bi-Metric Microplasty Line Extension
K142933 Biomet Tibial trays
K143009 Echo Bi-Metric Microplasty Hip System
Search all 404 clearances from BIOMET, INC. →