510(k) K871923

MICRO SCISSOR, 1.7MM by Arthropedics, Inc. — Product Code LRW

K871923 is an FDA 510(k) premarket notification submitted by Arthropedics, Inc. for the device "MICRO SCISSOR, 1.7MM". The FDA issued a decision of Substantially Equivalent on June 1, 1987. The device falls under product code LRW (Scissors, General, Surgical), a Class I device regulated under 21 CFR 878.4800. Arthropedics, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
June 1, 1987
Date Received
May 18, 1987
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Scissors, General, Surgical
Device Class
Class I
Regulation Number
878.4800
Review Panel
SU
Submission Type