510(k) K042897
K042897 is an FDA 510(k) premarket notification submitted by Ethicon Endo-Surgery, Inc. for the device "AUTOBAHN TISSUE CLOSURE DEVICE AND DISPOSABLE CARTRIDGE". The FDA issued a decision of Substantially Equivalent on November 19, 2004. The device falls under product code GAL (Suture, Absorbable, Natural), a Class II device regulated under 21 CFR 878.4830. Ethicon Endo-Surgery, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- November 19, 2004
- Date Received
- October 20, 2004
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Suture, Absorbable, Natural
- Device Class
- Class II
- Regulation Number
- 878.4830
- Review Panel
- SU
- Submission Type