510(k) K951860

HOWMEDICE BONE PLUG by Howmedica Corp. — Product Code LZN

K951860 is an FDA 510(k) premarket notification submitted by Howmedica Corp. for the device "HOWMEDICE BONE PLUG". The FDA issued a decision of SN on May 16, 1995. The device falls under product code LZN (Cement Obturator), a Class II device regulated under 21 CFR 878.3300. Howmedica Corp. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SN ()
Decision Date
May 16, 1995
Date Received
April 21, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Cement Obturator
Device Class
Class II
Regulation Number
878.3300
Review Panel
OR
Submission Type