510(k) K951860
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