510(k) K771708
- Device
- WORRELL PATELLA
- Applicant
- Depuy, Inc.
- 510(k) number
- K771708
- Product code
- HTG
- Decision
- Substantially Equivalent (SESE)
- Decision date
- 1977-10-06
- Date received
- 1977-09-12
- Regulation
- 888.3580
- Classification name
- Prosthesis, Knee, Hemi-, Patellar Resurfacing, Uncemented
- Medical specialty
- Orthopedic
- Review panel
- Orthopedic
- Device class
- 2
- Clearance type
- Traditional
- Third party reviewed
- N
Applicant Contact#
- Address
- 803 N. Front St. Suite 3 Mchenry IL US 60050 60050
FDA Registration Numbers#
- 3009732568
Source Documents#
510(k) summary PDF not indicated by FDA
Other 510(k) Records For Product Code HTG#
| 510(k) | Device | Applicant | Decision date |
|---|---|---|---|
| K800800 | PATELLAR COMPONENT FOR LUBINUS PATELLAR | Waldemar Link GmbH & Co. KG | 1980-04-21 |