The following data is part of a premarket notification filed by Vestil Manufacturing Corp. with the FDA for Frontier Model X5.
| Device ID | K030783 |
| 510k Number | K030783 |
| Device Name: | FRONTIER MODEL X5 |
| Classification | Wheelchair, Powered |
| Applicant | VESTIL MANUFACTURING CORP. 900 GROWTH PKWY. Angola, IN 46703 |
| Contact | Rick Michael |
| Correspondent | Rick Michael VESTIL MANUFACTURING CORP. 900 GROWTH PKWY. Angola, IN 46703 |
| Product Code | ITI |
| CFR Regulation Number | 890.3860 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2003-03-12 |
| Decision Date | 2003-04-04 |
| Summary: | summary |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| B391V60 | K030783 | 000 |
| 09356399000031 | K030783 | 000 |
| 09356399000024 | K030783 | 000 |
| 09356399000017 | K030783 | 000 |
| 09356399000000 | K030783 | 000 |