510(k) K830720

GRAF MENISCAL SUTURE SET by Acufex Microsurgical, Inc. — Product Code FZX

K830720 is an FDA 510(k) premarket notification submitted by Acufex Microsurgical, Inc. for the device "GRAF MENISCAL SUTURE SET". The FDA issued a decision of Substantially Equivalent on June 16, 1983. The device falls under product code FZX (Guide, Surgical, Instrument), a Class I device regulated under 21 CFR 878.4800. Acufex Microsurgical, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 16, 1983
Date Received
March 8, 1983
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Guide, Surgical, Instrument
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type