| Author(s)/Faculty: Charles K. Herman, MD | |||
| Type: Video | |||
| Release Date: 6/12/2015 | Expiration Date: 6/11/2016 | ||
| Credit Type: CME/Participation | Number of Credit(s): 0.25 | ||
CME Information
Support Statement: No commercial support for this activity.
Target Audience: The intended audience for this activity is plastic surgeons and other healthcare professionals involved in the treatment of plastic surgery patients.
Learning Objectives: Upon successful completion of this educational activity, participants should be better able to:
- Describe the design of the superolateral pedicle
- Identify techniques used to augment superior pole volume using this technique
Faculty:
Charles K. Herman, MD
Chairman, Department of Surgery
Director of Plastic Surgery
Pocono Health Systems
E. Stroudsburg, PA
This enduring material is approved for 2 years from the date of original release, June 12, 2015 to June 11, 2017.
External Reviewer
Seth R. Thaller, MD, DMD, FACS
Disclosures
In accordance with the Accreditation Council for Continuing Medical Education’s Standards for Commercial Support, all CME providers are required to disclose to the activity audience the relevant financial relationships of the planners, teachers, and authors involved in the development of CME content. An individual has a relevant financial relationship if he or she has a financial relationship in any amount occurring in the last 12 months with a commercial interest whose products or services are discussed in the CME activity content over which the individual has control.
Faculty members report the following relationship(s):
Charles K. Herman, MD
No relevant financial relationships to disclose.
External Reviewer reports the following relationship(s):
Seth R. Thaller, MD, DMD, FACS
No relevant financial relationships to disclose.
Unlabeled and Investigational Usage
The audience is advised that this continuing medical education activity may contain references to unlabeled uses of FDA-approved products or to products not approved by the FDA for use in the United States. The faculty members have been made aware of their obligation to disclose such usage. All activity participants will be informed if any speakers/authors intend to discuss either non-FDA approved or investigational use of products/devices.