510(k) K962971
K962971 is an FDA 510(k) premarket notification submitted by Davis & Geck, Inc. for the device "POLYPROPYLENE MESH (VARIOUS SIZES)". The FDA issued a decision of Substantially Equivalent on September 16, 1996. The device falls under product code FTL (Mesh, Surgical, Polymeric), a Class II device regulated under 21 CFR 878.3300. Davis & Geck, Inc. has at least 10 other 510(k) clearances on record.
Clearance Details
- Decision
- SESE (Substantially Equivalent)
- Decision Date
- September 16, 1996
- Date Received
- July 31, 1996
- Clearance Type
- Traditional
- Expedited Review
- No
- Third Party Review
- No
Device Classification
- Device Name
- Mesh, Surgical, Polymeric
- Device Class
- Class II
- Regulation Number
- 878.3300
- Review Panel
- SU
- Submission Type