Atlas FDA

MENISCAL REPAIR SYSTEM

FDA 510(k) clearance K853829 · decided 1985-10-08

Clearance details

K-number
K853829
Device name
MENISCAL REPAIR SYSTEM
Applicant
Concept, Inc.
Decision
Substantially Equivalent
Date received
1985-09-13
Decision date
1985-10-08
Days to decision
25 days
Clearance type
Traditional
Advisory committee
Unknown
Location
Clearwater, FL, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
HUNTER-SESSIONS VENA-CAVA OCCLUDER (P770005)Concept, Inc.1977-12-19