510(k) K021479
K021479 is an FDA 510(k) premarket notification submitted by Heinz Kurz GmbH Medizintechnik for the device "CLIP PISTON AWENGEN, MODEL# 1006 805 - 1006 861". The FDA issued a decision of Substantially Equivalent on May 21, 2002. The device falls under product code ETB (Prosthesis, Partial Ossicular Replacement), a Class II device regulated under 21 CFR 874.3450. Heinz Kurz GmbH Medizintechnik has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- May 21, 2002
- Date Received
- May 8, 2002
- Clearance Type
- Special
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Prosthesis, Partial Ossicular Replacement
- Device Class
- Class II
- Regulation Number
- 874.3450
- Review Panel
- EN
- Submission Type