ESPIN
Arthroscope
NLT SPINE LTD
The following data is part of a premarket notification filed by Nlt Spine Ltd with the FDA for Espin.
Pre-market Notification Details
| Device ID | K130057 |
| 510k Number | K130057 |
| Device Name: | ESPIN |
| Classification | Arthroscope |
| Applicant | NLT SPINE LTD 555 THIRTEENTH STREET NW Washington, DC 20004 |
| Contact | John J Smith |
| Correspondent | John J Smith NLT SPINE LTD 555 THIRTEENTH STREET NW Washington, DC 20004 |
| Product Code | HRX |
| CFR Regulation Number | 888.1100 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Special |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 2013-01-09 |
| Decision Date | 2013-02-07 |
| Summary: | summary |
Trademark Results [ESPIN]
Mark Image Registration | Serial | Company Trademark Application Date |
|---|---|
 ESPIN 87141185 5216868 Live/Registered |
ESPIN Inc. 2016-08-17 |
 ESPIN 76245983 not registered Dead/Abandoned |
Smith Technology Development, LLC 2001-04-24 |
 ESPIN 76245982 not registered Dead/Abandoned |
Smith Technology Development, LLC 2001-04-24 |
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