The following data is part of a premarket notification filed by Kls-martin L.p. with the FDA for Kls Martin Intraoral Zurich Ramus Distractor.
Device ID | K983809 |
510k Number | K983809 |
Device Name: | KLS MARTIN INTRAORAL ZURICH RAMUS DISTRACTOR |
Classification | External Mandibular Fixator And/or Distractor |
Applicant | KLS-MARTIN L.P. 3234 ELLA LN. New Port Richey, FL 34655 |
Contact | Ed Ransom |
Correspondent | Ed Ransom KLS-MARTIN L.P. 3234 ELLA LN. New Port Richey, FL 34655 |
Product Code | MQN |
CFR Regulation Number | 872.4760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1998-10-28 |
Decision Date | 1999-01-26 |
Summary: | summary |