510(k) K822367
K822367 is an FDA 510(k) premarket notification submitted by Treace Medical, Inc. for the device "TOTAL". The FDA issued a decision of Substantially Equivalent on September 7, 1982. The device falls under product code LBN (Replacement, Total Ossicular, Prosthesis, Porous, Polyethylene), a Class II device regulated under 21 CFR 874.3495. Treace Medical, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 7, 1982
- Date Received
- August 6, 1982
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Replacement, Total Ossicular, Prosthesis, Porous, Polyethylene
- Device Class
- Class II
- Regulation Number
- 874.3495
- Review Panel
- EN
- Submission Type