The following data is part of a premarket notification filed by Karl Storz Endoscopy-america, Inc. with the FDA for Model 28200c/shoulder/ankle/elbow/hip/tmj/sm Joint.
Device ID | K872986 |
510k Number | K872986 |
Device Name: | MODEL 28200C/SHOULDER/ANKLE/ELBOW/HIP/TMJ/SM JOINT |
Classification | Arthroscope |
Applicant | KARL STORZ ENDOSCOPY-AMERICA, INC. 10111 W. JEFFERSON BLVD. Culver City, CA 90232 -3578 |
Contact | Norman Silbertrust |
Correspondent | Norman Silbertrust KARL STORZ ENDOSCOPY-AMERICA, INC. 10111 W. JEFFERSON BLVD. Culver City, CA 90232 -3578 |
Product Code | HRX |
CFR Regulation Number | 888.1100 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1987-07-31 |
Decision Date | 1987-10-28 |