510(k) K931210

INTERMEDICS ORTHOPEDICS SAW BLADE by Intermedics Orthopedics — Product Code GFA

K931210 is an FDA 510(k) premarket notification submitted by Intermedics Orthopedics for the device "INTERMEDICS ORTHOPEDICS SAW BLADE". The FDA issued a decision of Substantially Equivalent on November 18, 1993. The device falls under product code GFA (Blade, Saw, General & Plastic Surgery, Surgical), a Class I device regulated under 21 CFR 878.4820. Intermedics Orthopedics has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 18, 1993
Date Received
March 10, 1993
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Blade, Saw, General & Plastic Surgery, Surgical
Device Class
Class I
Regulation Number
878.4820
Review Panel
SU
Submission Type